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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 247785생성일: 2026년 10월 26일

Benzoic acid, 4-((1-oxodecyl)oxy)- → 4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoate

https://huagongshe.com/reaction/247785

반응식

참여 물질

역할이름HCID투입량
반응물Benzoic acid, 4-((1-oxodecyl)oxy)-HCID 3608562—
반응물1,1,1-Trifluoro-2-decyl 4-hydroxybenzoateHCID 14745754—
용매TetrahydrofuranHCID 8028—
생성물4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoateHCID 19013920—

반응 단계

To a solution of the 4-n-decanoyloxybenzoic acid (0.4 g) obtained in (3) and the 1,1,1-trifluoro-2-decyl 4-hydroxybenzoate (0.4 g) obtained in (2) in tetrahydrofuran (about 30 ml) were added dicyclohexylcarbodiimide (0.32 g) and dimethylaminopyridine (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 (a developer : hexane/ethyl acetate=20/1) to obtain the titled compound (0.15 g). Phase transition temperatures (° C.) were observed under a polarization microscope using a hot stage as follows: ##STR53## where

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05207947
출처 데이터셋uspto-grants-1993_05
ORD IDord-6cfe97d6e01c4c83a1905e2fa8b45e0c
출처 메모uspto-grants-1993_05