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HRID 1726124作成日:2026年10月27日

(-)DIP-Chloride → (S)-4-[(4-bromophenyl)-hydroxymethyl]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1726124

反応式

関与物質

役割名称HCID仕込み量
反応物(-)DIP-ChlorideHCID 16212015—
反応物1-Boc-4-(4-Bromobenzoyl)piperidineHCID 22890526—
溶媒TetrahydrofuranHCID 8028—
生成物(S)-4-[(4-bromophenyl)-hydroxymethyl]-piperidine-1-carboxylic acid tert-butyl esterHCID 68970728—

反応手順

To a solution of (−)-DIP-chloride™ (6.42 g, 20.0 mmol) in THF (10 mL) at 0° C. was added 4-(4-bromobenzoyl)-piperidine-1-carboxylic acid tert-butyl ester (3.68 g, 10.0 mmol). The mixture was stirred at room temperature for 29 hours. Aqueous work-up and purification gave (S)-4-[(4-bromophenyl)-hydroxymethyl]-piperidine-1-carboxylic acid tert-butyl ester (ee 78% determined by both chiral HPLC and Mosher ester) as a crystalline solid (2.22 g, 54%). This material was recrystallized (CH2Cl2/hexane) three times to provide (S)-4-[(4-bromophenyl)-hydroxymethyl]-piperidine-1-carboxylic acid tert-butyl ester as a white solid (1.29 g, 35%) with ee of 96%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07491735B2
出典データセットuspto-grants-2009_02
ORD IDord-2eec1b163dc645e89f4a70ae50830d3b
出典メモuspto-grants-2009_02