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HRID 894486作成日:2026年10月25日
Ethyl 2-bromo-2-cyanoacetate → Ethyl 1-cyano-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylate
https://huagongshe.com/reaction/894486
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Ethyl 2-bromo-2-cyanoacetate | HCID 14469 | — |
| 反応物 | 1,3-Pentadiene, 1,1-dichloro-4-methyl- | HCID 108746 | — |
| 触媒 | Copper | HCID 23978 | — |
| 生成物 | Ethyl 1-cyano-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylate | HCID 12898169 | — |
反応手順
A mixture of 1,1-dichloro-4-methylpenta-1,3-diene (15.1 parts) ethylbromocyanoacetate (19.2 parts), copper-containing catalyst (as indicated in the table below), acid binder (as indicated in the table below) in solvent (as indicated in the table below; 100 parts by volume) is heated to the reflux temperature of the mixture if below 90° C., otherwise at a temperature not exceeding 90° C., and held at the reaction temperature for 6 hours. After removal of the solvent by distillation under reduced pressure the residue is extracted with a mixture of toluene (100 parts by volume), water (150 parts) and concentrated hydrochloric acid (100 parts by volume). The extract is filtered, the toluene layer is separated, washed with water (4×50 parts) and the crude ethyl-1-cyano-3-(2',2'-dichlorovinyl)-2,2-dimethylcyclopropane-1-carboxylate is isolated by distilling off the toluene under reduced pressure. The yield, strength and composition of the product obtained is given in the table below together with other reaction details.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04284582 |
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| 出典データセット | uspto-grants-1981_08 |
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| ORD ID | ord-63c8d51ddccc40f49691c52381e16091 |
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| 出典メモ | uspto-grants-1981_08 |
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