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HRID 1070875作成日:2026年10月25日

Benzyl Bromide → 6-[(2-Benzylmercapto-1-phenyl-1H-benzimidazol-6-yl)oxy]Hexanoic Acid Methyl Ester

https://huagongshe.com/reaction/1070875

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl BromideHCID 7498—
反応物Dicyclohexano-18-crown-6HCID 85955—
反応物Potassium BicarbonateHCID 516893—
反応物HCID 178500329HCID 178500329—
溶媒DimethylformamideHCID 6228—
生成物6-[(2-Benzylmercapto-1-phenyl-1H-benzimidazol-6-yl)oxy]Hexanoic Acid Methyl EsterHCID 69431600—

反応条件

温度20 °C

反応手順

490 mg of 6-[(2-mercapto-1-phenyl-1H-benzimidazol-6-yl)oxy]hexanoic acid methyl ester was dissolved in 7 ml of N,N-dimethylformamide, mixed with 0.19 ml of benzyl bromide, 278 mg of potassium bicarbonate and 49 mg of dicyclohexano-18-crown-6, and the mixture was stirred for 15 hours at 20° C. It was filtered, and the filtrate was concentrated by evaporation in a vacuum. The residue was purified by column chromatography on silica gel. 548 mg was obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06903126B2
出典データセットuspto-grants-2005_06
ORD IDord-b23502d5a8bc41d09c75a246a5547e42
出典メモuspto-grants-2005_06