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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1739186Generated: November 2, 2026

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

https://huagongshe.com/reaction/1739186

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 E above and using N-(3,4-dichlorophenyl)alanine (from Example B 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 numberUS05965614
Source datasetuspto-grants-1999_10
ORD IDord-b1a9de6601f94135a595fd96b820da42
Source noteuspto-grants-1999_10