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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405031Generated: October 25, 2026

Lithium Bromide → Methyl (S)-2-benzyloxycarbonylamino-4-oxo-5-phenylpentanoate

https://huagongshe.com/reaction/405031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium BromideHCID 82050—
ReactantMethyl (S)-2-benzyloxycarbonylamino-3-chlorocarbonylpropionateHCID 11055664—
ReactantHCID 178418336HCID 178418336—
SolventTetrahydrofuranHCID 8028—
ProductMethyl (S)-2-benzyloxycarbonylamino-4-oxo-5-phenylpentanoateHCID 5753534653.1%

Reaction Steps

To a suspension of copper(I) bromide-dimethyl sulfide complex (2.6 g, 12.72 mmol, 1.2 eq.) in dry THF was added a solution of lithium bromide (2.2 g, 25.44 mmol, 2.4 eq.) in dry THF. The mixture was stirred at room temperature (RT) for 20 min, and then was cooled to −78° C. A solution of benzyl magnesium chloride (13 mL, 12.72 mmol, 1.2 eq.) followed by a solution of (S)-methyl 2-(benzyloxycarbonylamino)-4-chloro-4-oxobutanoate (3.16 g, 10.6 mmol, 1 eq.) in dry THF were added. The mixture was stirred at −78° C. for 30 min and then was quenched with sat. ammonium chloride. The mixture was extracted with ethyl acetate. The organic layers were dried over magnesium sulfate and then concentrated in vacuo. The residue was purified by flash column (1:1 ethyl acetate:hexane) to give 2 g of (S)-methyl 2-(benzyloxycarbonylamino)-4-oxo-5-phenylpentanoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748649B2
Source datasetuspto-grants-2014_06
ORD IDord-8653999278ee4bb7ac3598bbcf43c7af
Source noteuspto-grants-2014_06