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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13751생성일: 2026년 10월 23일

Cyclohexanecarboxylic acid → 1-(2-Ethylbutyl)cyclohexanecarbonyl chloride

https://huagongshe.com/ko/reaction/13751

반응식

참여 물질

역할이름HCID투입량
반응물Cyclohexanecarboxylic acidHCID 7413—
반응물TributylamineHCID 7622—
반응물Thionyl ChlorideHCID 24386—
반응물1-(2-Ethyl-butyl)-cyclohexanecarboxylic acidHCID 10488751—
반응물1-(2-Ethyl-butyl)-cyclohexanecarboxylic acid anhydrideHCID 86612338—
생성물1-(2-Ethylbutyl)cyclohexanecarbonyl chlorideHCID 1065712595.8%

반응 조건

온도50 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728171B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-a6afc7c2b73440198c557ba7c96f00c6
출처 메모uspto-grants-2010_06