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HRID 1763955作成日:2026年10月27日
1,5-Diazabicyclo(4.3.0)non-5-ene → Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, ethyl ester
https://huagongshe.com/reaction/1763955
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | 1,5-Diazabicyclo(4.3.0)non-5-ene | HCID 76349 | — |
| 反応物 | Ethyl 2-(2,2-dichlorovinyl)-3,3-dimethyl-1-ethoxycarbonylcyclopropanecarboxylate | HCID 14914133 | — |
| 溶媒 | O-Xylene | HCID 7237 | — |
| 生成物 | Cyclopropanecarboxylic acid, 3-(2,2-dichloroethenyl)-2,2-dimethyl-, ethyl ester | HCID 101094 | 47.1% |
反応手順
13 g of diethyl 2,2-dimethyl-3-(2',2'-dichlorovinyl)-cyclopropane-1,1-dicarboxylate were dissolved in 50 g of o-xylene and 20 g of 1,5-diaza-bicyclo[4.3.0]non-5-ene were added. The mixture was then heated to the boil for 8 hours. After cooling, ice-cold dilute hydrochloric acid was added, so that a neutral or weakly acid pH value resulted. The organic phase was separated off and dried with Na2SO4 and the xylene was distilled off in vacuo (boiling point = 35° - 40° C./12 mm Hg). The residue weighed 12.5 g. Fractional distillation gave 4.7 g of 2,2-dimethyl-3-(2',2'-dichlorovinyl)-cyclopropane-1-carboxylic acid ethyl ester, of which 30% was in the cis form and 70% was in the trans form. The boiling point was 65° - 72° C./0.3 mm Hg. The nuclear magnetic resonance spectrum agreed with that given in the literature. 6.5 g of the starting material were recovered. The yield was thus 92%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04113969 |
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| 出典データセット | uspto-grants-1978_09 |
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| ORD ID | ord-78e28cdd9aae484aba09ec936786bc3d |
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| 出典メモ | uspto-grants-1978_09 |
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