戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 278218作成日:2026年10月27日

Benzyl chloroformate → Benzyl 4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/278218

反応式

関与物質

役割名称HCID仕込み量
反応物Benzyl chloroformateHCID 10387—
反応物DiisopropylethylamineHCID 81531—
反応物4-PiperidinemethanolHCID 420771—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物Benzyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 73649095.4%

反応手順

DIPEA (4.6 mL, 3.4 g, 26 mmol) was added to a solution of 4-(hydroxymethyl)piperidine (2.00 g, 17.4 mmol) dissolved in methylene chloride (20 mL). The solution was cooled in an ice bath and benzyl chloroformate (2.5 mL, 3.0 g, 18 mmol) was added dropwise over 10 min. After warming to rt and stirring for 96 h, the mixture was diluted with ethyl acetate (50 mL) and washed in succession with 25 mL each of saturated aq. sodium bicarbonate, 2N aq. HCl, saturated aq. sodium bicarbonate, and saturated aq. brine. The organic layer was dried (sodium sulfate), decanted, and evaporated to give 4.14 g of 1-(benzyloxycarbonyl)-4-(hydroxymethyl)piperidine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358979B1
出典データセットuspto-grants-2002_03
ORD IDord-7b25dbd6635246aea9e80cbaff47567b
出典メモuspto-grants-2002_03