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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 129801생성일: 2026년 10월 25일

Dimethyl Sulfoxide → (2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienal

https://huagongshe.com/reaction/129801

반응식

참여 물질

역할이름HCID투입량
반응물Dimethyl SulfoxideHCID 679—
반응물TriethylamineHCID 8471—
반응물Oxalyl chlorideHCID 65578—
반응물FarnesolHCID 445070—
용매Diethyl EtherHCID 3283—
용매DichloromethaneHCID 6344—
생성물(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienalHCID 5280598100.8%

반응 단계

To a CH2Cl2 solution (15 mL) of oxalyl chloride (7.81 mL, 87.7 mmol) was added dimethyl sulfoxide (12.5 mL, 175.4 mmol) dropwise over 30 min at -60° C. The resulting clear solution was stirred at this temperature for 20 min. A solution of trans, trans-farnesol (Aldrich Chemical Co.) (15 g, 67.5 mmol) in CH2Cl2 (325 mL) was added dropwise over 15 min. The reaction mixture became cloudy white during addition. The heterogeneous reaction mixture was stirred at -60° C. for 30 min, whereupon triethylamine (56.4 mL, 405 mmol) was added dropwise over 10 min. The reaction mixture became thick. The reaction mixture was allowed to warm to RT over 1 h. Ethyl ether (800 mL) was added and the organic layer was washed with H2O (500 mL), brine (500 mL) and dried over MgSO4. Evaporation gave 15 g (100%) of title compound as a crude oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05470845
출처 데이터셋uspto-grants-1995_11
ORD IDord-afa6e30a1fca4a3ebdbc57adcbef86cc
출처 메모uspto-grants-1995_11