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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1590356Generated: November 3, 2026

Ethyl bromoacetate → HCID 18322352, compound

https://huagongshe.com/reaction/1590356

Reaction equation

Participants

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

Reaction Steps

Among the methods for the preparation of the products of formula (A) above, there is described an O-alkylation 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, hereinafter designated COMPOUND 1, or the 2-[(7-carbethoxymethoxy-1,2,3,4-tetrahydronaphth-2-yl)-amino]-1-(3-chlorophenyl)ethanol, hereinafter designated COMPOUND 2. This reaction does not actually give good results because of the very low yield in final product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05202466
Source datasetuspto-grants-1993_04
ORD IDord-41b59a41d9a745b992aaef22f2f346b3
Source noteuspto-grants-1993_04