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HRID 247785作成日:2026年10月26日

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

https://huagongshe.com/reaction/247785

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoic acid, 4-((1-oxodecyl)oxy)-HCID 3608562—
反応物1,1,1-Trifluoro-2-decyl 4-hydroxybenzoateHCID 14745754—
溶媒TetrahydrofuranHCID 8028—
生成物4-(1,1,1-Trifluoro-2-decyloxycarbonyl)phenyl 4-n-decanoyloxybenzoateHCID 19013920—

反応手順

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

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05207947
出典データセットuspto-grants-1993_05
ORD IDord-6cfe97d6e01c4c83a1905e2fa8b45e0c
出典メモuspto-grants-1993_05