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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651414Generated: November 3, 2026

Ethyl bromoacetate → HCID 18322352, compound

https://huagongshe.com/reaction/1651414

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-phenylethanol 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 numberUS04927955
Source datasetuspto-grants-1990_05
ORD IDord-0d32398645b5404190f741c3d2709223
Source noteuspto-grants-1990_05