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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259605Generated: October 27, 2026

3-Aminobutanamide → 1-[p-(2-Methoxycarbonylaminovinyl)-phenoxy]-2-hydroxy-3-(2-carbamoyl-1-methyl-ethylamino)-propane

https://huagongshe.com/reaction/259605

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-AminobutanamideHCID 10931381—
Reactant1-[p-(2-Methoxycarbonylaminovinyl)-phenoxy]-2,3-epoxypropaneHCID 54361820—
SolventAcetonitrileHCID 6342—
Product1-[p-(2-Methoxycarbonylaminovinyl)-phenoxy]-2-hydroxy-3-(2-carbamoyl-1-methyl-ethylamino)-propaneHCID 54404419—

Reaction Steps

7.5 g (0.03 mol) of 1-[p-(2-methoxycarbonylaminovinyl)-phenoxy]-2,3-epoxypropane are dissolved in 75 ml of acetonitrile and added dropwise to a boiling stirred solution of 3.34 g (0.029 mol) of β-aminobutyric acid amide in 75 ml of acetonitrile. The mixture is stirred for 20 hours under reflux, the solvent is removed by distillation under reduced pressure and the oil which remains is partitioned between 350 ml of 0.1 N hydrochloric acid and 300 ml of ethyl acetate. The hydrochloric acid extract is separated off, rendered alkaline with sodium carbonate and extracted four times with 100 ml of ethyl acetate at a time. The organic phases are dried over sodium sulphate and evaporated under reduced pressure. The resulting oil yields 1-[p-(2-methoxycarbonylaminovinyl)-phenoxy]-2-hydroxy-3-(2-carbamoyl-1-methyl-ethylamino)-propane, of melting point 109°-111° C., from acetone-ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04038414
Source datasetuspto-grants-1977_07
ORD IDord-d52a38ae1a4a44f182182569b9798a20
Source noteuspto-grants-1977_07