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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 905300Generated: October 25, 2026

2-{[1,1-Dimethyl-2-(2-phenoxyacetamido)ethyl]amino}-2'-chloro-3',4'-bis(benzyloxy)acetophenone hydrobromide → 1,1-Dimethyl-2-(2-phenoxyacetamido)ethylamine

https://huagongshe.com/reaction/905300

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-{[1,1-Dimethyl-2-(2-phenoxyacetamido)ethyl]amino}-2'-chloro-3',4'-bis(benzyloxy)acetophenone hydrobromideHCID 20446758—
Reactant2-{[1,1-Dimethyl-2-(2-phenoxyacetamido)ethyl]amino}-2'-chloro-3',4'-dihydroxy acetophenone hydrobromideHCID 20446802—
Product1,1-Dimethyl-2-(2-phenoxyacetamido)ethylamineHCID 11806274—
Product3,4-Dibenzyloxyphenacyl bromideHCID 12681802—

Reaction Steps

The above acetophenone derivative (A) was itself prepared in 85% yield, as a solid m.p. 141°-143° C. by a similar procedure to that described for the equivalent starting material in Example 11, but from 2-{[1,1-dimethyl-2-(2-phenoxyacetamido)ethyl]amino}-2'-chloro-3',4'-bis(benzyloxy)acetophenone hydrobromide. The latter compound was itself obtained in 40% yield as a solid, m.p. 61°-63° C., from N-(2-amino-2-methylpropyl)-2-phenoxyacetamide and 2-bromo-3',4'-bis(benzyloxy)acetophenone using a procedure similar to that in Example 11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04423070
Source datasetuspto-grants-1983_12
ORD IDord-ebb36d08f9ca4acd92be7f997a9ed781
Source noteuspto-grants-1983_12