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HRID 3672作成日:2026年10月24日

Benzyl chloroformate → 2-{[(Benzyloxy)carbonyl]amino}-3-(thiophen-2-yl)propanoic acid

https://huagongshe.com/ja/reaction/3672

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Potassium CarbonateHCID 11430—
反応物2-ThienylalanineHCID 91444—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物2-{[(Benzyloxy)carbonyl]amino}-3-(thiophen-2-yl)propanoic acidHCID 1280683098%

反応手順

To a mixture of 3.0 g (16.9 mmol) of β-thienyl-D,L-alanine in 75 mL of water and 60 mL of dioxane, was added 5.6 g (40.6 mmol) of anhydrous potassium carbonate, followed by 2.85 mL (20 mmol) of carbobenzyloxychloride. The resulting mixture was stirred rapidly for approximately one hour. When the reaction was substantially complete, as indicated by thin layer chromatography (21/7/7/9, EtOAc/AcOH/CH3 CN/H2O), the reaction mixture was concentrated. The resultant layers were separated and the aqueous layer was washed with 75 mL of diethyl ether and then layered with 150 mL of methylene chloride. The resultant mixture was acidified with rapid stirring to pH=2.0 using 5N hydrochloric acid. The layers were then separated, and the organic layer was dried with sodium sulfate (Na2SO4), filtered and concentrated to provide 5.05 g of desired compound (98%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05734057
出典データセットuspto-grants-1998_03
ORD IDord-608e80bb9092458b8ead7e8d78854485
出典メモuspto-grants-1998_03