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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467312Generated: October 31, 2026

Ethyl bromoacetate → HCID 18322352, compound

https://huagongshe.com/reaction/467312

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 numberUS05159103
Source datasetuspto-grants-1992_10
ORD IDord-29eccfc366284d08b93f9a4896bd5502
Source noteuspto-grants-1992_10