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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247782생성일: 2026년 10월 25일

Chloride → Benzoic acid, 4-(phenylmethoxy)-, 1-(trifluoromethyl)nonyl ester

https://huagongshe.com/reaction/247782

반응식

참여 물질

역할이름HCID투입량
반응물ChlorideHCID 312—
반응물2-DimethylaminopyridineHCID 21885—
반응물4-BenzyloxybenzoylchlorideHCID 3766410—
반응물1,1,1-Trifluorodecan-2-olHCID 3864464—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물Benzoic acid, 4-(phenylmethoxy)-, 1-(trifluoromethyl)nonyl esterHCID 1474575396.3%

반응 단계

To a solution of 4-benzyloxybenzoic acid chloride (1.23 g) in methylene chloride (10 ml) was slowly added under ice cooling a solution of optically active 1,1,1-trifluoro-2-decanol (0.96 g), dimethylaminopyridine (0.55 g) and triethylamine (0.48 g) in methylane chloride (20 ml). The mixture was left to stand until it reached room temperature and allowed to react overnight. The mixture was poured in ice water and extracted with methylene chloride. The extracted layer was washed with dilute aqueous hydrochloric acid solution, water, 1N aqueous sodium carbonate solution and water in this order, and was dried over anhydrous magnesium sulfate. After the solution was distilled to remove the solvent, the crude product thus obtained was purified by toluene-silica-gel column chromatography and recrystallized from ethanol to obtain the titled compound (1.84 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05207947
출처 데이터셋uspto-grants-1993_05
ORD IDord-859e072770fa41648e889dcb531ae8cb
출처 메모uspto-grants-1993_05