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HRID 6331作成日:2026年10月24日

tert-Butyl hydroperoxide → 2,3-Difluoro-4-octyloxyphenyl 4-hexyloxybenzoate

https://huagongshe.com/ja/reaction/6331

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl hydroperoxideHCID 6410—
反応物DicyclohexylcarbodiimideHCID 10868—
反応物2-DimethylaminopyridineHCID 21885—
反応物4-(Hexyloxy)benzoic acidHCID 70834—
反応物2,3-Difluoro-4octyloxyphenolHCID 14766703—
反応物2,3-DifluorooctyloxybenzeneHCID 19103632—
反応物CID 86747250HCID 86747250—
反応物ButyllithiumHCID 178418339—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物2,3-Difluoro-4-octyloxyphenyl 4-hexyloxybenzoateHCID 19103718—

反応手順

0.1 mol of 4-hexyloxybenzoic acid, 0.01 mol of dimethylaminopyridine and 0.1 mol of 2,3-difluoro-4octyloxyphenol (preparable from 2,3-difluorooctyloxybenzene by lithiation at -70° to -80° and dropwise addition of a solution of lithium t-butylperoxide in ether prepared from 0.12 mol of t-butyl hydroperoxide and 0.12 mol of butyllithium) are introduced into 150 ml of dichloromethane, a solution of 0.1 mol of dicyclohexylcarbodiimide in 30 ml of dichloromethane is added dropwise with stirring at 10o, and the mixture is subsequently stirred at room temperature for 15 hours. The mixture is filtered through silica gel, the solvent is evaporated, and 2,3-difluoro-4-octyloxyphenyl 4-hexyloxybenzoate is obtained as the residue.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248447
出典データセットuspto-grants-1993_09
ORD IDord-82e83c02b9134508a72b2b79ba90c519
出典メモuspto-grants-1993_09