| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 121 | PROCESSES FOR PREPARING 1-CYCLOPROPYL-5-PHENYL-PENTANE-2,4-DION DERIVATIVES AND THEIR INTERMEDIATES, AND THE NEW INTERMEDIATES | HU0102096 | 1999-03-22 | HU0102096A2 | 2002-03-28 | CRAMP SUSAN MARY; GEACH NEIL JONATHAN |
| 122 | ID20002121 | 1999-03-22 | ID27440A | 2001-04-12 | CRAMP SUSAN MARY; GEACH NEIL JONATHAN | |
| 123 | Fluorinated alkanes and their uses | DE19719280 | 1997-05-07 | DE19719280C1 | 1998-09-24 | MENZ DIRK-HENNING DR |
| 124 | METHOD OF PRODUCING ANILINE LABELLED WITH TRITIUM | SU3745159 | 1984-05-24 | SU1219585A1 | 1986-03-23 | NEFEDOV VLADIMIR D; TOROPOVA MARGARITA A; SIMONOVA TAMARA P; AVRORIN VIKTOR V; ZHURAVLEV VLADIMIR E |
| 125 | PROCEDIMIENTO PARA PREPARAR COMPUESTOS HERBICIDAS DE TIPO ARILOXIBENCENOCARBONIMIDA | ES534196 | 1984-07-11 | ES8601862A1 | 1985-11-01 | |
| PROCEDIMIENTO PARA PREPARAR COMPUESTOS HERBICIDAS DE TIPO ARILOXIBENCENOCARBONIMIDA. CONSISTE EN: HACER REACCIONAR UN HALOGENURO DE IMIDOILO DE FORMULA (II) CON UN COMPUESWTO DE FORMULA R3OM1, A UNA TEMPERATURA DE 10 A 150 C Y EN UN DISOLVENTE DE FORMULA R3OH PARA OBTENER UN COMPUESTO DE FORMULA (I). SIENDO: R1, UN GRUPO X2R3 O NR4R5; R2, H, HAL Y OTROS; R3, ALQUILO, ALILO Y OTROS; R4, H, ALQUILO Y OTROS; R5, COMO R4 O CATION Y OTROS; W, Y, Y, X, Z,, H, HAL Y OTROS; X2 UN ATOMO DE OXIGENO, O DE AZUFRE; M1, UN ATOMO DE HIDROGENO, O UN ATOMO DE METAL ALCALINO. SE UTILIZA COMO HERBICIDA DE POST-EMERGENCIA PARA DICOTILEDONEAS EN CULTIVOS DE SOJA. | ||||||
| 126 | X-METHYL-(6-PHENOXY)-2-PICOLYL CYCLOPROPANECARBOXYLATES | IE7685 | 1985-01-11 | IE850076L | 1985-07-12 | |
| 127 | EXTRACTION OF HALOCENATED HYDROCARBONS FROM AQUEOUS SOLUTIONS USING PHOSPHINE OXIDES ON INERT SUPPORTS AS THE EXTRACTANT | ZA837305 | 1983-09-29 | ZA837305B | 1984-05-30 | BRIGHT JOHN HARVEY; AJIT KUMAR CHAUDHURI; SAVIDES CHRISTOS |
| 128 | CH507378 | 1978-05-10 | CH640207A5 | 1983-12-30 | VERBRUGGE PIETER ADRIAAN; TERLOUW WILLEM; KRAMER PETRUS ANTHONIUS | |
| 129 | PREPARATION OF DIHALOCYCLOPROPANE CONTAINING ESTERS AND HYDROCARBONS | AU3598878 | 1978-05-10 | AU3598878A | 1979-12-06 | VERBRUGGE PIETER ADRIAAN; TERLOUW WILLEM; KRAMER ANTHONIUS |
| 130 | RO7799074 | 1974-03-12 | RO64264A2 | 1979-03-15 | RADULY-BAKA LAJOS; CURCANEANU STEFAN; DIMITRIU IUSTIN; LAZARUT PETRU; LUCACIU NICOLAE | |
| 131 | A process for the preparation of derivatives dihalogencyclopropan | DE2820410 | 1978-05-10 | DE2820410A1 | 1978-11-16 | VERBRUGGE PIETER ADRIAAN; TERULOUW WILLEM; KRAMER PETRUS ANTHONIUS |
| 132 | Preparation of dihalocyclopropaanderivaten. | NL7804900 | 1978-05-08 | NL7804900A | 1978-11-14 | |
| 133 | PL18286975 | 1975-08-22 | PL97556B1 | 1978-03-30 | ||
| 134 | PROCESS FOR OXYHALOGENATION OF HYDROCARBONS AND/OR THEIR DERIVATIVES | IN1973CA1974 | 1974-09-03 | IN143087B | 1977-10-01 | JOSEPH J |
| 135 | Apparatus for the production of chlorinated hydrocarbons by means of molten salts | DE2651865 | 1976-11-13 | DE2651865A1 | 1977-06-02 | SZE MORGAN C |
| 136 | DD19441475 | 1975-08-22 | DD125480A5 | 1977-04-20 | ||
| 137 | LU73238A1 - | LU73238 | 1975-08-21 | LU73238A1 | 1977-04-15 | |
| 138 | RO7394872 | 1972-02-23 | RO61681A2 | 1977-03-15 | ||
| 139 | PROCESS FOR THE CONTINUOUS PRODUCTION OF MONOCHLOROALKANES AND MONOCHLOROCYCLOALKANES | GB2950775 | 1975-07-14 | GB1457710A | 1976-12-08 | |
| 1457710 Monochloro-alkanes and -cycloalkanes DEUTSCHE TEXACO AG 14 July 1975 [20 July 1974] 29507/75 Heading C2C Monochloro-alkanes or -cycloalkanes containing more than 4C atoms and with the Cl atom bonded to a specific C atom are prepared in a continuous process by reacting the corresponding alcohol with HCl in the presence of aqueous ZnCl 2 solution as catalyst by passing a thin layer of a mixture saturated with HCl and containing 1À5-3 parts by weight of a conc. aqueous ZnCl 2 solution containing at least 50% by weight zinc chloride and 1 part by weight of the alcohol downwardly at a temperature of at least 50 C. through a reactor of large-internal surface area and passing sufficient gaseous HCl in countercurrent to the solution that an excess of HCl amounting to at least 5% based on the amount of HCl required for complete reaction of the alcohol, is available. The reactor is preferably a heat exchanger or a column or tower fitted with trays or packing. In the examples monochlorocyclohexane and 1-chlorododecane are prepared. | ||||||
| 140 | FR2090071B1 - | FR7117660 | 1971-05-14 | FR2090071B1 | 1976-12-03 | |
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