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HRID 374535생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/374535

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl chloroformateHCID 10387—
반응물Potassium CarbonateHCID 11430—
반응물2-ThienylalanineHCID 91444—
반응물EtOAc AcOH CH3CN H2OHCID 131719237—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물2-{[(Benzyloxy)carbonyl]amino}-3-(thiophen-2-yl)propanoic acidHCID 1280683098%

반응 단계

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, ethyl acetate/acetic acid/acetonitrile/water), 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 sodium sulfate (Na2SO4), filtered and concentrated to provide 5.05 g of desired compound (98%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05480887
출처 데이터셋uspto-grants-1996_01
ORD IDord-c7f3fc7a4e744d51ba5908cef44464ab
출처 메모uspto-grants-1996_01