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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 21427생성일: 2026년 10월 25일

Triethylamine → (R)-(+)-1,1,1-trifluoro-2-octyl 4-benzyloxybenzoate

https://huagongshe.com/reaction/21427

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물2-DimethylaminopyridineHCID 21885—
반응물(R)-(+)-1,1,1-Trifluoro-2-octanolHCID 2779099—
반응물4-BenzyloxybenzoylchlorideHCID 3766410—
용매DichloromethaneHCID 6344—
생성물(R)-(+)-1,1,1-trifluoro-2-octyl 4-benzyloxybenzoateHCID 2285073061.2%

반응 단계

To a solution of 4-benzyloxybenzoic acid chloride (4.3 g) in methylene chloride (50 ml) was added a solution of (R)-(+)-1,1,1-trifluoro-2-octanol (2.9 g) ([α]D22.5 =+20.1, optical purity 96.3 % ee), dimethylaminopyridine (0.6 g) and triethylamine (1.7 g) in methylene chloride (50 ml) under ice-cooling. The mixture was left to stand at the room temperature for 24 hours before being poured in ice water. The methylene chloride layer separated was washed with diluted hydrochloric acid, water, 1N aqueous sodium carbonate solution and water in this order before being dried over magnesium sulfate. After distillation was over purification by toluene/silica gel chromatography and recrystallization from ethanol gave the titled compound (3.8 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05424005
출처 데이터셋uspto-grants-1995_06
ORD IDord-85bfe5171bf14946843aa1a406d7b425
출처 메모uspto-grants-1995_06