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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5252생성일: 2026년 10월 23일

Water → (Z)-9-octadecenoic acid 4-[(tetrahydro-2H-pyran-2-yl)oxy]butyl ester

https://huagongshe.com/ko/reaction/5252

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Cesium carbonateHCID 10796—
반응물Oleic AcidHCID 445639—
반응물2-(4-Bromobutoxy)tetrahydro-2H-pyranHCID 559019—
용매TetrahydrofuranHCID 8028—
생성물(Z)-9-octadecenoic acid 4-[(tetrahydro-2H-pyran-2-yl)oxy]butyl esterHCID 67857132100%

반응 단계

To a stirring solution of 2.0 g (7.0 mmol) of oleic acid and 1.6 g (7.0 mmol) of 2-(4-bromobutoxy)tetrahydro-2H-pyran in 20 mL of tetrahydrofuran is added 2.3 g (7.1 mmol) of cesium carbonate and the reaction mixture is stirred overnight at room temperature. The reaction mixture is poured into water and extracted with three 100 mL portions of ether. The combined organic layers are dried over MgSO4 and concentrated in vacuo affording 2.9 g (100%) of (Z)-9-octadecenoic acid 4-[(tetrahydro-2H-pyran-2-yl)oxy]butyl ester. Next, 500 mg of Dowex 50W 8X resin is added to a stirring solution of 2.9 g (7.0 mmol) of (Z)-9-octadecenoic acid 4-[(tetrahydro-2H-pyran-2-yl)oxy]butyl ester in 100 mL of 1:1 tetrahydrofuran/methanol and the reaction mixture is stirred overnight at room temperature. The reaction mixture is filtered and concentrated in vacuo affording 2.4 g (100%) of alcohol. Next, 11 mL of 2.0M Jones reagent is added at 0° C. to a stirring solution of 2.4 g (7.0 mmol) of alcohol in 75 mL of acetone and the reaction mixture is stirred for 2 hours. The reaction mixture is poured into water and extracted with three 50 mL portions of ether. The combined organic layers are dried over MgSO4 and concentrated in vacuo affording 2.1 g (81%) of title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05242945
출처 데이터셋uspto-grants-1993_09
ORD IDord-29b460b072c94947be0258f84aeee882
출처 메모uspto-grants-1993_09