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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 233339생성일: 2026년 10월 24일

Hydrochloric Acid → methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)carbamate

https://huagongshe.com/ko/reaction/233339

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물BromochloromethaneHCID 6333—
반응물ChlorotrimethylsilaneHCID 6397—
반응물(S)-Methyl 2-((methoxycarbonyl)amino)-3-phenylpropanoateHCID 10609905—
반응물HCID 178506865HCID 178506865—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)carbamateHCID 988153370%

반응 단계

15.4 ml of a 2.6 molar solution of hexyllithium in hexane were added dropwise at -80° C. to a solution of 9.50 g of methyl (S)-2-methoxycarbonylamino-3-phenyl-propionate in 60 ml of tetrahydrofuran. Subsequently, the mixture was treated with 5.60 ml of chlorotrimethylsilane. The resulting suspension was stirred and treated with 3.22 ml of bromochloromethane. Subsequently, 18.4 ml of hexyllithium solution were added. The solution was treated at -80° C. with 11 ml of 20% methanolic hydrochloric acid, warmed to 22° and diluted with 100 ml of water and 40 ml of tetrahydrofuran. The phases were separated and the organic phase was washed with saturated sodium chloride solution, dried and concentrated. The residue was recrystallized from ethyl acetate and hexane and the crystallizate was dried, there being obtained 7.20 g (70%) of pure methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate, m.p. 122°-123° C. IR (KBr): 3336s (NH), 1737s and 1686s (C=O), 1535s (amide II).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05591885
출처 데이터셋uspto-grants-1997_01
ORD IDord-9bef9ffaabdf42c7983198d7d20b557d
출처 메모uspto-grants-1997_01