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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380603Generated: November 3, 2026

Allyl bromide → 2-Methyl-2-(morpholin-4-yl)-1-{4-[(prop-2-en-1-yl)sulfanyl]phenyl}propan-1-one

https://huagongshe.com/reaction/1380603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methyl-2-(morpholin-4-yl)-1-(4-sulfanylphenyl)propan-1-oneHCID 15702404—
SolventAcetoneHCID 180—
Product2-Methyl-2-(morpholin-4-yl)-1-{4-[(prop-2-en-1-yl)sulfanyl]phenyl}propan-1-oneHCID 23325681—

Reaction Steps

10 g (0.38 mol) of 1-(4-mercaptophenyl)-2-methyl-2-morpholinopropan-1-one, 5 g (0.041 mol) of freshly distilled allylbromide and 5.2 g (0.038 mol) of dry potassium carbonate are suspended in 50 ml of acetone and the mixture is heated to reflux temperature for 16 hours. After cooling, the solvent is removed by distillation, water and diethyl ether are added to the residue, and the water phase is extracted with ether. The organic phase is washed with 10% NaOH solution and water, dried over MgSO4 and concentrated. The oil which remains is distilled in a bulb tube at 180°-200° C./13 Pa. (Compound No. 23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04582862
Source datasetuspto-grants-1986_04
ORD IDord-b82f6e8826624f98bc1f243d34221af4
Source noteuspto-grants-1986_04