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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 4541Generated: October 28, 2026

2-(Oxiran-2-ylmethoxy)benzonitrile → 1-[2-(3-Carbamoyl-4-hydroxyphenoxy)-1,1-dimethylethylamino]-3-(2-cyanophenoxy)propan-2-ol

https://huagongshe.com/reaction/4541

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Oxiran-2-ylmethoxy)benzonitrileHCID 12619671—
Reactant5-(2-Amino-2-methylpropoxy)salicylamideHCID 13754425—
Solvent1,4-DioxaneHCID 31275—
Product1-[2-(3-Carbamoyl-4-hydroxyphenoxy)-1,1-dimethylethylamino]-3-(2-cyanophenoxy)propan-2-olHCID 13754382—

Reaction Steps

The solution of 2.24 g of 5-(2-amino-2-methylpropoxy)salicylamide in 30 ml of dioxan is refluxed for 7 hours after the addition of 2.3 g of 2-(2,3-epoxypropoxy)benzonitrile, and then concentrated by evaporation. The residue is divided between 10 ml of 2N hydrochloric acid and 100 ml of ethyl acetate. The acidic aqueous phase is rendered alkaline with concentrated ammonia solution, the base is extracted with ethyl acetate and the solvent is evaporated off, whereupon an oil is obtained from which, by crystallisation from isopropanol and recrystallisation from ethyl acetate, 1-[2-(3-carbamoyl-4-hydroxyphenoxy)-1,1-dimethylethylamino]-3-(2-cyanophenoxy)propan-2-ol having a melting point of 125°-126° is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04727067
Source datasetuspto-grants-1988_02
ORD IDord-5b74e8a69c9c4ca0b289ab0ce493c1ed
Source noteuspto-grants-1988_02