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HRID 71775作成日:2026年10月23日

4-Piperidinecarboxylic acid → 1-Carbobenzoxy-4-piperidinecarboxylic Acid

https://huagongshe.com/ja/reaction/71775

反応式

関与物質

役割名称HCID仕込み量
反応物4-Piperidinecarboxylic acidHCID 3773—
反応物Benzyl chloroformateHCID 10387—
反応物Sodium HydroxideHCID 14798—
溶媒WaterHCID 962—
生成物1-Carbobenzoxy-4-piperidinecarboxylic AcidHCID 73648991.2%

反応条件

温度0 °C

反応手順

Piperidine-4-carboxylic acid (64.8 g, 0.5 mol) in H2O (50 mL) was treated with NaOH (44.0 g, 1.1 mol). The reaction mixture was cooled to 0° C. and treated with CbzCl (93.8 g, 0.55 mol). The reaction mixture was stirred at ambient temperature for 4 hours and the mixture was extracted with Et2O (3 150 mL). The aqueous phase was acidified with 6 N HCl (140 mL) and extracted with EtOAc (3 200 mL). The solution was dried over MgSO4, filtered, and concentrated to afford crude piperidine-1,4-dicarboxylic acid monobenzyl ester (120 g), which was used without further purification: MS (ESI) m/z 262 [M−H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822430B2
出典データセットuspto-grants-2014_09
ORD IDord-faee25c567534f6e93cd002eea407fee
出典メモuspto-grants-2014_09