참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Pentachlorophenol | HCID 992 | — |
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Phosphorus pentachloride | HCID 24819 | — |
| 반응물 | alpha-Cyanobenzeneacetic acid | HCID 26403 | — |
| 용매 | Carbon Tetrachloride | HCID 5943 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | alpha-Cyano-phenylacetic acid pentachlorophenylester | HCID 20402417 | — |
반응 단계
8 g. (0.05 moles) of α-cyano-phenylacetic acid are dissolved in 80 ml. of dichloromethane, 10.2 g. (0.05 moles) of phosphorous pentachloride are added and the mixture is stirred for 2 hours at the boiling point of the dichloromethane. The reaction is completed when the hydrochloric acid evolution ceases. The solvent is distilled off and the residue containing the obtained acid chloride and phosphoroxychloride is taken up in carbontetrachloride and the solution is added dropwise to 13 g. (0.05 moles) of pentachlorophenol and 4 ml. (0.05 moles) of pyridine dissolved in 200 ml. of carbontetrachloride. The reaction mixture is cooled and the precipitated pyridine chlorohydrate is removed by washing twice with 50 ml. of water, dried, distilled off and the residue is distilled off with diisopropyl ether. The precipitated crystalline product is cooled and filtered. The α-cyanophenylacetic acid pentachlorophenyl ester is air-dried.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04508658 |
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| 출처 데이터셋 | uspto-grants-1985_04 |
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| ORD ID | ord-43ffbc2a2594471d80d70c227c2d8036 |
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| 출처 메모 | uspto-grants-1985_04 |
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