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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462359Generated: October 26, 2026

2-Amino-1-(4-benzyloxyphenyl)ethanol → 4-benzyloxy-alpha-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-ethyl]-aminomethyl]-benzyl alcohol

https://huagongshe.com/reaction/1462359

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-1-(4-benzyloxyphenyl)ethanolHCID 423990—
Reactant6-(2-Bromoethoxy)-2,2-dimethyl-2,3-dihydro-4H-1,3-benzoxazin-4-oneHCID 13754413—
Product4-benzyloxy-alpha-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-ethyl]-aminomethyl]-benzyl alcoholHCID 54167698—

Reaction Steps

A mixture of 21 g of α-(aminomethyl)-4-benzyloxybenzyl alcohol and 12 g of 6-(2-bromoethoxy)-2,3-dihydro-2,2-dimethyl-4H-1,3-benzoxazin-4-one is stirred in an oil bath at 130° for 1 hour. The reaction mixture is partitioned between 500 ml of ethyl acetate and 50 ml of 2N aqueous ammonia solution, the organic phase is separated off and evaporated and the residue is recrystallised from isopropanol. 4-Benzyloxy-α-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-ethyl]-aminomethyl]-benzyl alcohol with a melting point of 160°-162° is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04460580
Source datasetuspto-grants-1984_07
ORD IDord-cc76c75f99254711af56e75a59fbb1d5
Source noteuspto-grants-1984_07