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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2248985Generated: October 29, 2026

Ethyl bromoacetate → HCID 18322352, compound

https://huagongshe.com/reaction/2248985

Reaction equation

Participants

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

Reaction Steps

Among the methods of preparation of the products of formula (A) hereinabove there is described an O-alkylation that, starting from the 2-[(7-hydroxy-1,2,3,4-tetrahydronaphth-2-yl)amino]-1-phenyl-ethanol or from the 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 give yet good result because the yield of the final product is very low.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05041606
Source datasetuspto-grants-1991_08
ORD IDord-cdc227b8ded74855b837d9436bf7470c
Source noteuspto-grants-1991_08