Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419055Generated: November 2, 2026

3-[N-[4-chloro-2-[2-benzyloxy-alpha-hydroxybenzyl]phenyl]-N-isobutylcarbamoyl]acrylic acid → 5-Chloro-alpha-(2-ethoxyphenyl)-2-isobutylaminobenzyl alcohol

https://huagongshe.com/reaction/1419055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[N-[4-chloro-2-[2-benzyloxy-alpha-hydroxybenzyl]phenyl]-N-isobutylcarbamoyl]acrylic acidHCID 69945939—
SolventEthanolHCID 702—
Product5-Chloro-alpha-(2-ethoxyphenyl)-2-isobutylaminobenzyl alcoholHCID 54042866—

Reaction Steps

In 150 ml of ethanol was dissolved 6.0 g of ethyl ester of 3-[N-[4chloro-2-[2-benzyloxy-α-hydroxybenzyl]phenyl]-N-isobutylcarbamoyl]acrylic acid, as obtained in (4), to which was added 3.18 g of potassium carbonate; the mixture was then stirred overnight. The solvent was distilled off under reduced pressure, and the residue was subjected to extraction with 150 ml of water and 200 ml of ethyl acetate. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate, then distilled off under reduced pressure. The residue was purified by means of silica gel column chromatography (eluent, hexane:ethyl acetate=5:1) to yield 5.8 g of ethyl ester of trans-5-(2-benzyloxyphenyl)-7-chloro-1-isobutyl-2-oxo-1,2,3,5-tetrahydro-4,1-benzoxazepine-3-acetic acid as prism crystals, m.p. 146° to 147° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885979
Source datasetuspto-grants-1999_03
ORD IDord-7ba50abba7fc4fb78fb61c0ed565d88e
Source noteuspto-grants-1999_03