Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1462375Generated: November 1, 2026

Isopropanol → alpha-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-1,1-dimethyl-ethyl]-aminomethyl]-benzyl alcohol

https://huagongshe.com/reaction/1462375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantStyrene OxideHCID 7276—
Reactant5-(2-Amino-2-methylpropoxy)salicylamideHCID 13754425—
Solvent1,4-DioxaneHCID 31275—
Productalpha-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-1,1-dimethyl-ethyl]-aminomethyl]-benzyl alcoholHCID 54496208—

Reaction Steps

A solution of 4.5 g of 5-(2-amino-2-methyl-propoxy)-salicylamide and 3.1 g of 2-phenyloxirane in 40 ml of dioxane is refluxed for 16 hours. The solvent is subsequently evaporated off under reduced pressure, and the residue is dissolved in 20 ml of 2N hydrochloric acid, and extracted with 50 ml of ether. The water phase is separated; it is rendered alkaline with concentrated ammonia, and the liberated base is extracted with 200 ml of ethyl acetate. Customary further processing yields a light-coloured foam, from which is obtained, by recrystallisation from isopropanol, α-[N-[2-(3-carbamoyl-4-hydroxy-phenoxy)-1,1-dimethyl-ethyl]-aminomethyl]-benzyl alcohol, m.p. 121°-123°. It forms a neutral fumarate, m.p. 209°-210° (from methanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04460580
Source datasetuspto-grants-1984_07
ORD IDord-9b886e1594624d82980d314f142ad3c6
Source noteuspto-grants-1984_07