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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2292852Generated: October 30, 2026

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

https://huagongshe.com/reaction/2292852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBromochloromethaneHCID 6333—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant(S)-Methyl 2-((methoxycarbonyl)amino)-3-phenylpropanoateHCID 10609905—
ReactantHCID 178506865HCID 178506865—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Productmethyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)carbamateHCID 988153370%

Reaction Steps

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 hexyllithlum solution were added. The solution was treated at -80° C. with 11 ml of 20% methanolic hydrochloric acid, warmed to 220 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-oxopropyl)-carbamate, m.p. 122°-123° C. IR (KBr): 3336s (NH), 1737s and 1686s (C=O), 1535s (amide II).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05684176
Source datasetuspto-grants-1997_11
ORD IDord-4283e600b56340ec9a6340c69c66f573
Source noteuspto-grants-1997_11