Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983452Generated: October 26, 2026

Water → (+/-)-[3-[bis(phenylmethyl)amino]-2-hydroxypropyl]-2(1H)pyrimidinone

https://huagongshe.com/reaction/983452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
ReactantN,N-dibenzyl-1-(oxiran-2-yl)methanamineHCID 11276836—
ReactantHCID 178479648HCID 178479648—
SolventMethanolHCID 887—
SolventTolueneHCID 1140—
Product(+/-)-[3-[bis(phenylmethyl)amino]-2-hydroxypropyl]-2(1H)pyrimidinoneHCID 2256081845%

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of 2-hydroxypyrimidine hydrochloride (1:1) (0.075 mol) in methanol (150 ml) was stirred for 30 minutes and then added to a solution of sodium carbonate (0.075 mol) in methanol (20 ml). The mixture was stirred and refluxed for 15 minutes, and cooled to 55° C. A solution of N,N-bis(phenylmethyl)oxiranmethanamine (0.075 mol) in toluene (160 ml) was added dropwise and the reaction mixture was stirred at 50° C. overnight. Water (75 ml) was added and the mixture was stirred at 55° C. for 15 minutes. The organic layer was separated, washed with water, dried, filtered and the solvent was evaporated. The residue was purified by column chromatography over silica gel (eluent: CH3OH/CH2Cl2 97/3). The pure fractions were collected and the solvent was evaporated, yielding 11.8 g (45%) of (±)-1-[3-[bis(phenylmethyl)amino]-2-hydroxypropyl]-2(1H)pyrimidinone (interm. 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864273B1
Source datasetuspto-grants-2005_03
ORD IDord-9eb688e745404af191d496479c6c7af9
Source noteuspto-grants-2005_03