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HRID 17864作成日:2026年10月24日

Nipecotic Acid → 1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acid

https://huagongshe.com/ja/reaction/17864

反応式

関与物質

役割名称HCID仕込み量
反応物Nipecotic AcidHCID 4498—
反応物Benzyl chloroformateHCID 10387—
反応物Sodium HydroxideHCID 14798—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物1-((Benzyloxy)carbonyl)piperidine-3-carboxylic acidHCID 234339—

反応手順

To an ice cooled solution of nipecotic acid (10.0 g, 77.5 mmol), sodium hydroxide (3.4 g, 85 mmol), and tetrahydrofuran (50 mL) in water (100 mL) was added by simultaneous dropwise addition benzylchloroformate (13.3 mL, 93 mmol) in tetrahydrofuran (50 mL) and sodium hydroxide (3.4 g, 85 mmol) in water (50 mL). Warmed slowly to room temperature. After 24 hours tetrahydrofuran was removed in vacuo and the resulting aqueous mixture acidified with 3 N hydrochloric acid and extracted with dichloromethane (3×). The combined organic portions were dried with anhydrous magnesium sulfate. Filtration followed by evaporation of the filtrate in vacuo gave the titled compound. 1HNMR (CHCl3, 300 MHz) □ 7.45-7.20 (m, 5H); 5.14 (m, 2H); 4.21 (br s, 1H); 3.96 (m, 1H), 3.15 (br s, 1H); 2.93 (m, 1H); 2.51 (m, 1H); 2.09 (m, 1H); 1.80-1.60 (m, 2H); 1.50 (m, 1H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741322B2
出典データセットuspto-grants-2010_06
ORD IDord-41a63700f6cc44a0b5ecf557890effc5
出典メモuspto-grants-2010_06