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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841103Generated: October 30, 2026

tert-Butyl bromoacetate → N-(3,4-dichlorophenyl)alanine Tert-butyloxycarbonylmethyl Ester

https://huagongshe.com/reaction/1841103

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl bromoacetateHCID 79177—
ReactantN-(3,4-dichlorophenyl)alanineHCID 5491659—
ProductN-(3,4-dichlorophenyl)alanine Tert-butyloxycarbonylmethyl EsterHCID 54406316—

Reaction Steps

Following General Procedure AE above and using N-(3,4-dichlorophenyl)alanine (from Example AB above) and tert-butyl bromoacetate (Aldrich), the title compound was prepared as a solid. The reaction was monitored by silica gel tlc (Rf=0.57 in 25% EtOAc/hexanes). Purification was by recrystallization from ethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06683075B1
Source datasetuspto-grants-2004_01
ORD IDord-0efcf723fc0d4466840c0f296bae83a6
Source noteuspto-grants-2004_01