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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1267856생성일: 2026년 10월 27일

Benzyl chloroformate → (2S)-2-{[(benzyloxy)carbonyl]amino}-2-methylpentanedioic acid

https://huagongshe.com/reaction/1267856

반응식

참여 물질

역할이름HCID투입량
반응물Benzyl chloroformateHCID 10387—
반응물2-Methylglutamic acidHCID 95440—
용매Sodium HydroxideHCID 14798—
생성물(2S)-2-{[(benzyloxy)carbonyl]amino}-2-methylpentanedioic acidHCID 2068120583%

반응 단계

To a stirred solution of α-methyl-D,L-glutamic acid (10 g, 62 mmol) in 2 N sodium hydroxide (62 mL) at 0.5° C. was added benzyl chloroformate (12.7 g, 74.4 mmol) over 30 min. After the addition was complete the reaction mixture was stirred at room temperature for 3 hours. During, this time the pH was maintained at 11 by addition of 2N sodium hydroxide (33 mL). The reaction mixture was then extracted with ether (60 mL). The aqueous layer was cooled in an ice bath and then acidified with 4N hydrochloric acid (34 mL) to pH=1. The resulting mixture was extracted with ethyl acetate (3×100 mL). The combined ethyl acetate extracts were washed with brine (60 mL) and dried (MgSO4). The solvent was removed in vacuo to give 15.2 g (83%) of N-benzyloxycarbonyl-α-methylglutamic acid as an oil: 1H NMR (CDCl3) δ 8.73(m, 5H), 5.77(b, 1H), 5.09(s, 2H), 2.45-2.27(m, 4H), 2.0(s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06555554B2
출처 데이터셋uspto-grants-2003_04
ORD IDord-1467c5a528f1437a9ac43defa4ba8421
출처 메모uspto-grants-2003_04