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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254382Generated: November 1, 2026

Ethyl bromoacetate → HCID 18322352, compound

https://huagongshe.com/reaction/2254382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantHCID 129948HCID 129948—
ReactantHCID 129953HCID 129953—
ProductHCID 18322352HCID 18322352—

Reaction Steps

Among the preparative methods of the products of formula (A) hereinabove, an O-alkylation is described that, starting from 2-[(7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenylethanol or from 2-[(7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-(3-chlorophenyl)ethanol, by reaction with ethyl bromoacetate gives the 2-[(7-carbethoxymethoxy-1,2,3,4-tetrahydronaphth-2-yl)-amino]-1-phenylethanol or the 2-[(7-carbethoxymethoxy-1,2,3,4-tetrahydronaphth-2-yl)-amino]-1-(3-chlorophenyl)ethanol. This reaction does not actually give good results because the yield in end product is very low.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05235103
Source datasetuspto-grants-1993_08
ORD IDord-ec895d6090f040528fdcc3be7e8e32b0
Source noteuspto-grants-1993_08