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HRID 48124作成日:2026年10月24日

2-Dimethylaminopyridine → 2',3'-difluoro-4'-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethyl-heptyloxycarbonyl]-phenyl ester

https://huagongshe.com/ja/reaction/48124

反応式

関与物質

役割名称HCID仕込み量
反応物2-DimethylaminopyridineHCID 21885—
反応物4-hydroxybenzoic acid (R)-1-trifluoromethyl-heptyl esterHCID 14549217—
反応物2',3'-Difluoro-4'-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-biphenyl-4-carboxylic acidHCID 22016254—
溶媒TetrahydrofuranHCID 8028—
溶媒DiisopropylcarbodiimideHCID 12734—
生成物2',3'-difluoro-4'-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethyl-heptyloxycarbonyl]-phenyl esterHCID 8675937365%

反応手順

To a solution of 2′,3′-difluoro-4′-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-biphenyl-4-carboxylic acid (14 A) (1 equi.), (4-hydroxy benzoic acid (R)-1-trifluoromethyl-heptyl ester (7) (1 equi.), and DMAP (dimethylaminopyridine) (0.1 equi.) in THF (25 mL/mmole), DIC (diisopropyl carbodiimide) (1.2 equi.) was added at room temperature. The reaction mixture was stirred at that temperature for 24 h, quenched with water, extracted with ethyl acetate:hexane(1:1), washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by chromatography on silica gel (5% EtOAc/hexanes) gave 2′,3′-difluoro-4′-(5,5,6,6,7,7,8,8,8-nonafluoro-octyloxy)-biphenyl-4-carboxylic acid 4-[(R)-1-trifluoromethyl-heptyloxycarbonyl]-phenyl ester (15A) as a white solid (65%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703082B1
出典データセットuspto-grants-2004_03
ORD IDord-7244747d2dfe4650a008e9fa1afb83a6
出典メモuspto-grants-2004_03