참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cyclohexanecarboxylic acid | HCID 7413 | — |
| 반응물 | Tributylamine | HCID 7622 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid | HCID 10488751 | — |
| 반응물 | 1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid anhydride | HCID 86612338 | — |
| 생성물 | 1-(2-Ethylbutyl)cyclohexanecarbonyl chloride | HCID 10657125 | 95.8% |
반응 단계
A mixture of 103.0 mmol 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid, 38.9 mmol cyclo-hexanecarboxylic acid and 173 μL tributylamine (0.71 mmol=0.005 eq. relative to the sum of both acids) was warmed to 50° C. 12.4 mL (170.3 mmol=1.2 Eq. relative to the sum of both acids) of thionyl chloride was added during 16 minutes at a temperature of 44-51° C. (reaction is endothermic, vigorous gas evolution) and the reaction mixture was kept at 53-55° C. After 15 minutes the reaction was complete (0.08% 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid and no 1-(2-ethyl-butyl)-cyclohexanecarboxylic acid anhydride). After removing volatile components in vacuo (60° C. bath, 2.7-1.9 mbar followed by 120° C. bath, 8.8-13 mbar) 24.86 g of the residue was obtained (assay 95.8% 1-(2-ethyl-butyl)-cyclohexanecarbonyl chloride, yield 100%).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728171B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-a6afc7c2b73440198c557ba7c96f00c6 |
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| 출처 메모 | uspto-grants-2010_06 |
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