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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247788생성일: 2026년 10월 23일

1,1,1-Trifluoro-2-decyl 4-hydroxybenzoate → Benzoic acid, 4-((1-oxodecyl)oxy)-

https://huagongshe.com/ko/reaction/247788

반응식

참여 물질

역할이름HCID투입량
반응물1,1,1-Trifluoro-2-decyl 4-hydroxybenzoateHCID 14745754—
반응물4-(1,1,1-Trifluoro-2-octyloxycarbonyl)phenyl 4-n-decanoyloxybenzoateHCID 19764212—
용매TetrahydrofuranHCID 8028—
생성물Benzoic acid, 4-((1-oxodecyl)oxy)-HCID 3608562—
생성물4-(1,1,1-Trifluoro-2-octyloxycarbonyl)phenyl 4-n-decanoyloxybenzoateHCID 19764212—

반응 단계

To a solution of the 4-n-decanoyloxybenzoic acid (0.43 g) obtained in Example 12, (3) and the 1,1,1-trifluoro-2-octyl 4-hydroxybenzoate (0.4 g) obtained in (2) above in tetrahydrofuran (about 30 ml) were added dicyclohexylcarbodiimide (0.32 g) and dimethylamonopyridine (0.01 g). The mixture was stirred at room temperature for about 20 hours and was distilled to remove the solvent. The residue was dissolved in dichloromethane and washed with water. The organic layer was dried over anhydrous magnesium sulfate and was distilled to remove the solvent. The residue was purified by silica-gel column chromatography (developer : hexane/ ethyl acetate=20/1) to obtain the titled compound (0.20 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05207947
출처 데이터셋uspto-grants-1993_05
ORD IDord-76d2acb9c9be47e299d7228a7db3f18a
출처 메모uspto-grants-1993_05