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HRID 323165作成日:2026年10月26日

(4-Carboxybutyl)triphenylphosphonium bromide → 4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(5-carboxy-1-pentenyl)phenyl]benzamide

https://huagongshe.com/reaction/323165

反応式

関与物質

役割名称HCID仕込み量
反応物(4-Carboxybutyl)triphenylphosphonium bromideHCID 161236—
反応物4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-formylphenyl)benzamideHCID 22010987—
反応物Potassium tert-butoxideHCID 23665647—
溶媒Ethyl AcetateHCID 8857—
溶媒DimethylacetamideHCID 31374—
生成物4-(4'-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(5-carboxy-1-pentenyl)phenyl]benzamideHCID 7006873167.7%

反応手順

To an ice bath cooled solution of (4-carboxybutyl)triphenylphosphonium bromide (371 mg) in N,N-dimethylacetamide (15 ml) was added potassium t-butoxide (188 mg) and the mixture was stirred at the same temperature for 30 minutes. To the resulting mixture was added 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-(2-formylphenyl)benzamide (250 mg) and the mixture was stirred in an ice bath for 3 hours. The mixture was diluted with ethyl acetate (40 ml) and the solution was washed successively with 1N hydrochloric acid (30 ml), water (20 ml) and brine (20 ml). The organic phase was dried over magnesium sulfate and the solvent was evaporated in vacuo to give an oil. The crude oil was purified by silica gel column (1% methanol in chloroform) to give 4-(4′-methylbiphenyl-2-carboxamido)-N-methyl-N-[2-(5-carboxypenten-1-yl)phenyl]benzamide (201 mg) as a colorless amorphous.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06211242B1
出典データセットuspto-grants-2001_04
ORD IDord-8da00f1b70e04d54a83cc5747f0c5e8c
出典メモuspto-grants-2001_04