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HRID 1066856作成日:2026年10月27日

tert-Butyl N-(4-hydroxybutyl)carbamate → N-(t-butoxycarbonyl)-4-(2-fluoro-5-bromobenzyloxy)butylamine

https://huagongshe.com/reaction/1066856

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl N-(4-hydroxybutyl)carbamateHCID 545141—
反応物4-Bromo-2-(bromomethyl)-1-fluorobenzeneHCID 13553295—
反応物Potassium tert-butoxideHCID 23665647—
溶媒TetrahydrofuranHCID 8028—
生成物N-(t-butoxycarbonyl)-4-(2-fluoro-5-bromobenzyloxy)butylamineHCID 21196003—

反応条件

温度-40 °C

反応手順

In a 25 ml flask 4-(t-butoxycarbonylamino)butanol was dissolved in tetrahydrofuran (15 ml) under a nitrogen atmosphere. The solution was cooled to −40° C. and potassium tert-butoxide (1M in tetrahydrofuran, 2.14 ml, 2.14 mmol) was added slowly. The resulting mixture was stirred at −40° C. for thirty minutes. To this reaction mixture was added 2-fluoro-5-bromobenzyl bromide (521 mg, 1.94 mmol), added dropwise as a solution in tetrahydrofuran (3.5 ml). The resulting mixture was slowly warmed to 0° C. and stirred at this temperature for two hours. The progress of the reaction was monitored by thin layer chromatography. The reaction mixture was partitioned between 1 M potassium carbonate and methylene chloride. The aqueous fraction was back-extracted with methylene chloride. The organic fractions were combined and dried over sodium sulfate. The solvents were removed in vacuo. The desired intermediate was further purified by liquid chromatography.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06245761B1
出典データセットuspto-grants-2001_06
ORD IDord-d3a78e57ef244b938203929a695e2ad2
出典メモuspto-grants-2001_06