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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116594Generated: October 25, 2026

2-(4-Chlorophenoxy)ethylamine → Ethyl{[({2-[(4-chlorophenyl)oxy]ethyl}-amino)carbonyl]oxy}acetate

https://huagongshe.com/reaction/2116594

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-Chlorophenoxy)ethylamineHCID 2794191—
ReactantEthyl [(phenoxycarbonyl)oxy]acetateHCID 12094709—
SolventTolueneHCID 1140—
ProductEthyl{[({2-[(4-chlorophenyl)oxy]ethyl}-amino)carbonyl]oxy}acetateHCID 91288841—

Reaction Steps

A solution of 0.6 g (3.5 mmol) of [(4-chloro-phenyl)oxy]ethylamine (Chim. Ther. 1973, 8, 259-270) and 1.3 g (5.8 mmol) of ethyl [(phenyloxy-carbonyl)oxy]acetate, prepared in Step 1.1., in 30 ml of toluene is heated at 60° C. overnight. It is evaporated to dryness and the product is purified by chromatography on silica gel, eluting with a 30/70 mixture of ethyl acetate and cyclohexane. This gives 0.7 g of oily product, containing ˜10% of cyclized oxazolidine dione product, used as it is in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439257B2
Source datasetuspto-grants-2008_10
ORD IDord-ed6b8fecc7394dd98990156476ad2dc3
Source noteuspto-grants-2008_10