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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 26796Generated: October 26, 2026

Ethyl chloroformate → Ethyl 2-{{4-{2-[2-(3-methoxyphenoxy)-2-methylpropionylamino]-ethyl}-phenoxy}}-2-methylpropionate

https://huagongshe.com/reaction/26796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant2-(3-Methoxyphenoxy)-2-methylpropanoic acidHCID 3781663—
ReactantEthyl 2-[4-(2-aminoethyl)-phenoxy]-2-methylpropionateHCID 19356632—
SolventTriethylamineHCID 8471—
ProductEthyl 2-{{4-{2-[2-(3-methoxyphenoxy)-2-methylpropionylamino]-ethyl}-phenoxy}}-2-methylpropionateHCID 2132271384%

Reaction Steps

In a manner analogous to that described in Example 4, from 2-(3-methoxyphenoxy)-2-methylpropionic acid and ethyl 2-[4-(2-aminoethyl)-phenoxy]-2-methylpropionate, in the presence of triethylamine and ethyl chloroformate, there is obtained, in a yield of 84% of theory, ethyl 2-{{4-{2-[2-(3-methoxyphenoxy)-2-methylpropionylamino]-ethyl}-phenoxy}}-2-methylpropionate which, after recrystallization from cyclohexane and ethyl acetate, melts at 68°-69° C. and from this 2-{{4-{2-[2-(3-methoxyphenoxy)-2-methylpropionylamino]-ethyl}-phenoxy}}-2-methylpropionic acid in a yield of 64% of theory which, after recrystallization from cyclohexane and ethyl acetate, melts at 80°-81° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04151303
Source datasetuspto-grants-1979_04
ORD IDord-a8b6ce499f984df08f2513e2f827ea46
Source noteuspto-grants-1979_04