| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 1 | 均三甲苯磺酸盐组合物及其方法 | CN201380080831.8 | 2013-11-13 | CN105705485A | 2016-06-22 | D·R·斯盖翁; 阿伦·阿加瓦尔; 大卫·E·达布尼; 格雷戈里·P·达多; 拉斐特·D·弗兰德; 舒曼·密特拉; 杰奎琳·M·皮特尔; W·L·史密斯; E·斯则克雷斯; 迈克尔·R·特里; 肯尼斯·L·维埃拉 |
| 本发明涉及组合物，这些组合物包含次卤酸盐或次氯酸和2,4,6均三甲苯磺酸盐的可溶性盐。这些组合物可以包含表面活性剂、缓冲剂、或其组合。其他助剂也可以存在。此类组合物不需要包含高浓度的氢氧化钠或其他可溶性氢氧化物盐以大幅度增加pH(以及因此稳定性)，尽管此类氢氧化物可以存在，如果希望的话。 | ||||||
| 2 | 烷烃的光诱导的催化C-H氧化 | CN202080081186.1 | 2020-09-27 | CN114901626A | 2022-08-12 | A·M·斯皮尔曼; S·K·桑特拉 |
| 提供了一种氧化苄基C‑H键的方法。该方法包括引发剂的光诱导活化和随后与氧的反应，导致自由基的形成。随后，自由基催化苄基C‑H键与氧的反应，从而形成含氧化合物。 | ||||||
| 3 | 五氟苯氧基化合物、使用该化合物的非水电解液以及锂二次电池 | CN200680056312.8 | 2006-11-08 | CN101535237B | 2013-04-24 | 安部浩司; 桑田孝明; 高濑学 |
| 本发明提供一种新型的五氟苯基化合物及其制造方法、以及可以形成电容量、循环特性、保存特性等电池特性优异的锂二次电池的非水电解液和锂二次电池。本发明是下述通式(I)表示的五氟苯氧基化合物、及其制造方法以及含有该化合物的非水电解液和锂二次电池，式中，R1表示-COCO-基、S＝O基或S(＝O)2基，R2表示烷基、环烷基、链烯基、炔基、芳基或芳烷基，其中，R2所含有的氢原子中的1个以上可以被卤原子取代，R1为-COCO-基时，R2不包含芳基。 | ||||||
| 4 | 一种甘油直接制备环氧丙醇的方法 | CN201310134991.8 | 2013-04-17 | CN103214402A | 2013-07-24 | 郑丽萍; 侯昭胤; 潘赛勇; 陈平 |
| 本发明涉及一种化学制备方法，具体地说，是一种甘油直接制备环氧丙醇的方法。本发明的技术方案是在玻璃或者搪瓷反应釜中，放入混合溶剂，将甘油加入上述混合溶剂，控制甘油在反应液中的浓度为0.5-3.0摩尔/升，然后加入催化剂，控制催化剂的量为甘油重量的0.01-0.20；将上述混合好的反应液在搅拌条件下，升温至40-100度，恒温反应2-20小时；反应后，反应液过滤除去催化剂，然后将液体反应混合液蒸馏，收取160-161度区间的馏分，即得到产品2,3-环氧丙醇。本发明的技术方案具有原料价廉、催化剂易得可循化、零排放、过程绿色等显著优点，同时，易操作控制、产率较高，产品纯度高，工艺运行成本低，为工业化生产提供了新的思路。 | ||||||
| 5 | 五氟苯氧基化合物、使用该化合物的非水电解液以及锂二次电池 | CN200680056312.8 | 2006-11-08 | CN101535237A | 2009-09-16 | 安部浩司; 桑田孝明; 高濑学 |
| 本发明提供一种新型的五氟苯基化合物及其制造方法、以及可以形成电容量、循环特性、保存特性等电池特性优异的锂二次电池的非水电解液和锂二次电池。本发明是下述通式(I)表示的五氟苯氧基化合物、及其制造方法以及含有该化合物的非水电解液和锂二次电池，式中，R1表示－COCO－基、S＝O基或S(＝O)2基，R2表示烷基、环烷基、链烯基、炔基、芳基或芳烷基，其中，R2所含有的氢原子中的1个以上可以被卤原子取代，R1为－COCO－基时，R2不包含芳基。 | ||||||
| 6 | Method for preparing polythiol compound and polymeric composition for optical material comprising same | US14402573 | 2013-05-23 | US09522879B2 | 2016-12-20 | Dong Gyu Jang; Soo Gyun Roh; Jong Hyo Kim |
| The present invention relates to novel methods for preparing a polythiol compound for use in an optical material and polymerizable compositions including a polythiol compound prepared by the methods. According to the methods, a polythiol compound with uniform color, high purity and high quality can be prepared at reduced cost. The polymerizable compositions can be used to manufacture clear, transparent optical lenses with good heat resistance and excellent optical properties. | ||||||
| 7 | SULFONIUM SALT AND PHOTO-ACID GENERATOR | US14289686 | 2014-05-29 | US20140357896A1 | 2014-12-04 | Issei Suzuki; Takuya Ikeda; Yusaku Takashima; Takeshi Furuta; Yoshitaka Komuro; Yoshiyuki Utsumi; Takaaki Kaiho; Toshiaki Hato |
| Provided is a novel sulfonium salt that has high solubility in a solvent and has high light sensitivity to, especially, light having a wavelength not longer than deep-UV (254 nm) and a novel photo-acid generator comprising the sulfonium salt. The invention relates to a sulfonium salt represented by the following general formula (1) and a novel photo-acid generator comprising the sulfonium salt. wherein R1 represents an electron withdrawing group; R2 and R3 each independently represent an alkyl group having 1 to 5 carbon atoms, an alkoxy group, an acyl group, a halogenated alkyl group, a halogen atom, a hydroxyl group, a cyano group, or a nitro group; p and q each independently represent an integer of 0 to 5; and X− represents a monovalent counter anion. | ||||||
| 8 | 2-ethoxy-3-phenyl propanoic acid derivatives for the treatment of lipid disorders | JP2006516441 | 2004-06-16 | JP2006527752A | 2006-12-07 | リンドステット−アルスターマーク，エヴァ−ロッテ |
| 式中、TがO、S又はNRを表し、Rが水素、C 1-6アルキル基又はフェニルC 1-6アルキル基を表す場合の式Iの化合物及びその医薬として許容できる塩、このような化合物の製造方法、インスリン耐性に関連する又は関連しない脂質障害（異常脂質血症）を含む臨床症状を治療するのにそれらの化合物の有用性、これらの化合物の治療用途方法、及びこれらの化合物を含有する医薬組成物。 | ||||||
| 9 | Method for producing aromatic amine compound and amination agent for aromatic compound | JP2004212062 | 2004-07-20 | JP2006028127A | 2006-02-02 | SANO SATOSHI; TAKEUCHI KIYOSHI |
| <P>PROBLEM TO BE SOLVED: To provide an efficient method for producing an aromatic amine compound with a simple process in high yield, and to obtain a new amination agent for an aromatic compound. <P>SOLUTION: The method for producing the aromatic amine compound expressed by formula (III) comprises the reaction of a compound expressed by formula (I) with a compound expressed by formula (II) in the presence of an acid and the hydrolysis of the reaction product. This amination agent for the aromatic compound is expressed by formula (II). In these formulas, R<SB>1</SB>is a substituent; (n) is an integer of 0-5; when (n) is an integer of 2-5, a plurality of the R<SB>1</SB>groups may be the same or different or bonded together to form a ring; R<SB>2</SB>and R<SB>3</SB>are each independently a substituted or unsubstituted alkyl; R<SB>2</SB>and R<SB>3</SB>may be bonded together to form a ring; and Q is a heterocyclic group, an acyl group, an aryloxycarbonyl group, an alkoxycarbonyl group, phosphonyl group, sulfamoyl group, an alkylsulfonyl group or an arylsulfonyl group. <P>COPYRIGHT: (C)2006,JPO&NCIPI | ||||||
| 10 | Insecticidal n- (optionally substituted) n'-substituted -n, n'-disubstituted hydrazine | JP9548787 | 1987-04-20 | JP2767241B2 | 1998-06-18 | ADAMU CHAIITANGU SHU; DONARUDO UESUREI HAMUPU |
| 11 | Pentafluorophenyloxy compound, and nonaqueous electrolyte and lithium secondary cell using the same | JP2005304850 | 2005-10-19 | JP2007112737A | 2007-05-10 | ABE KOJI; KUWATA TAKAAKI; TAKASE MANABU |
| <P>PROBLEM TO BE SOLVED: To provide a new pentafluorophenyl compound and a method for producing the compound, to provide a nonaqueous electrolyte capable of forming a lithium secondary cell excellent in cell properties such as electric capacity, cycling characteristics and preservation characteristics, and to provide a lithium secondary cell. <P>SOLUTION: The pentafluorophenyloxy compound is represented by formula (I). The nonaqueous electrolyte and the lithium secondary cell, comprising the compound, are provided. Wherein, R<SP>1</SP>is -COCO-, S=O, or S(=O)<SB>2</SB>; and R<SP>2</SP>is an alkyl, a cycloalkyl, an alkenyl, an alkynyl, an aryl or an aralkyl, wherein one or more H in R<SP>2</SP>may be substituted with a halogen atom and, when R<SP>1</SP>is -COCO-, R<SP>2</SP>contains no aryl. <P>COPYRIGHT: (C)2007,JPO&INPIT | ||||||
| 12 | Menadione choline bisulfite adduct and its manufacturing method | JP26394685 | 1985-11-26 | JPH0670000B2 | 1994-09-07 | ハンス・キーフアー; ヨアヒム・ウー・シユナイダー |
| 13 | Acylation of nephthalene compound | JP5384788 | 1988-03-09 | JPS63301842A | 1988-12-08 | ANBUROGIO MAGUNI; GIUZETSUPINA BIZENCHIN |
| 14 | Preparation of epsilon-guanidino-n-caproic acid p-ethoxycarbonylphenyl ester or its acid addition salt | JP16246983 | 1983-09-02 | JPS6054352A | 1985-03-28 | ADACHI TSUTOMU; TAKAHASHI KINOKAZU; TAKAHASHI YOSHIO; TAMURA TOSHIAKI |
| PURPOSE: To obtain the titled compound useful as a remedy for pancreatitis, by reacting a p-hydroxybenzoic acid derivative with ε-guanidino-n-caproic acid. CONSTITUTION: A compound shown by the formula is reacted with ε-guanidino- n-caproic acid or its acid addition salt in a solvent such as benzene, ether, etc. under cooling at icecold W room temperature, preferably in the presence of a base (e.g., phridine, or triethylamine), to give the desired compound. The compound shown by the formula is obtained by reacting thionyl chloride with p- hydroxybenzoic acid ethyl ester in the presence of a base in a solvent. COPYRIGHT: (C)1985,JPO&Japio | ||||||
| 15 | Novel phenol process for preparing same and stabilized organic material containing same | JP4311277 | 1977-04-14 | JPS52128359A | 1977-10-27 | SAMIYUERU EBANSU |
| 16 | Pentafluorophenyloxy compound, a non-aqueous electrolyte and lithium secondary battery using the same | JP2005304850 | 2005-10-19 | JP4961714B2 | 2012-06-27 | 浩司 安部; 孝明 桑田; 学 高瀬 |
| 17 | Acid amide derivative, method for producing the same and pesticide containing the same | JP2009030652 | 2009-02-13 | JP2009143951A | 2009-07-02 | NAKAMURA YUJI; MORITA MASAYUKI; YONEDA TETSUO; IZAKURA KENJI |
| <P>PROBLEM TO BE SOLVED: To provide a pesticide having an extremely high controlling effect on pests in a low medicinal amount, and hardly exerting bad influence to mammalian animals, fishes and the like. <P>SOLUTION: The pesticide contains an acid amide derivative expressed by formula (I) [wherein A represents benzyl which may be substituted with X, naphtyl which may be substituted with X or the like; B represents phenyl which may be substituted with Y, furyl which may be substituted with Y or the like; X represents a halogen, an alkyl, a haloalkyl or the like; Y represents a halogen, an alkyl, a haloalkyl or the like; R<SB>1</SB>and R<SB>2</SB>represent each an alkyl, cyano or the like; R<SB>3</SB>represents H], or its salt. <P>COPYRIGHT: (C)2009,JPO&INPIT | ||||||
| 18 | Koruhinoru derivatives as vascular damaging agents | JP2000592241 | 1999-12-24 | JP2002534400A | 2002-10-15 | アルヌール，ジャン−クロード; デイビス，ピーター・デビッド; ボイル，フランシス・トーマス |
| (57)【要約】 本発明は、人などの温血動物において血管損傷作用を生じさせるのに使用するための薬剤の製造に於ける式(I)： 【化１】 [式中、Xは-C(O)-、-C(S)-、-C=NOHまたは-CH(R 7 )-であり、ここでR 7は水素、ヒドロキシ、C 1-7アルコキシ、-OR 8または-NR 8 R 9 [ここで、R 8は基-Y 1 R 10 (ここで、Y 1は直接結合、-C(O)-、-C(S)-、-S-、-C(O)O-、-C(O)NR 11 -、-SO 2 -または-SO 2 NR 12 -(ここで、R 11及びR 12は、同一または異なっていてもよく、それぞれ独立して、水素、C 1-3アルキルまたはC 1-3アルコキシC 2-3アルキルである)であり、R 10は本明細書中の定義通りである）であり、R 9は水素である]であり；R 1 、R 2及びR 3は本明細書中の定義通りであり、好ましくはメチルであり；R 4 、R 5及びR 6は、本明細書中の定義通りであり、但し、R 5はヒドロキシ、アルコキシ、置換アルコキシ、-OPO 3 H 2 、-OC 1-7アルカノイル、ベンジルオキシを除く]の化合物及びその塩の使用に関する。 本発明はさらに、式(I)の化合物、かかる化合物を含有する医薬組成物及び、人などの温血動物で血管損傷作用を生じさせるために前記化合物を使用する処置方法に関する。 式(I)の化合物及びその医薬的に許容可能な塩は、癌及びリウマチ様動脈炎などの多くの症状の処置に有用である。 | ||||||
| 19 | Insecticidal n-(optionally substituted)-n'- substituted-n,n'-disubstituted hydrazine | JP9548787 | 1987-04-20 | JPS63267752A | 1988-11-04 | ADAMU CHIYAIITANGU SHIYU; DONARUDO UESUREI HAMUPU |
| 20 | Menadione choline biphosphite adduct and manufacture | JP26394685 | 1985-11-26 | JPS61143345A | 1986-07-01 | YOAHIMU UU SHIYUNAIDAA; HANSU KIIFUAA |
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