Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1683367Generated: November 2, 2026

Acetone → HCID 18323177, compound

https://huagongshe.com/reaction/1683367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBenzenesulfenyl chlorideHCID 11008040—
Reactant4‐Methyl‐2‐(methylsulfanyl)‐4‐phenyl‐4,5‐dihydro‐ 1H‐imidazol‐5‐oneHCID 18323165—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18323177HCID 18323177—

Reaction Steps

0.6 g (2.7 mmol) of 2-methylthio-4-methyl-4-phenyl-2-imidazolin-5-one in solution in 50 ml of anhydrous tetrahydrofuran (THF) is charged to a 100 ml, three-necked, round-bottomed flask under an inert atmosphere. The solution is stirred with a magnetic stirrer and is cooled to 0° C. (ice bath+acetone). 0.30 g (1 molar equivalent) of potassium tert-butoxide is added and the mixture is stirred for 10 minutes at 0° C. A solution containing 0.40 g of phenylsulfenyl chloride (phenylthio chloride) and 10 ml of anhydrous THF is then run in. The mixture is then left to return to room temperature for one hour. The reaction mixture is run into 100 ml of water. Extraction is carried out with 100 ml of ethyl acetate. The organic phase is washed 4 times with water and dried over sodium sulfate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05637729
Source datasetuspto-grants-1997_06
ORD IDord-90118db2d33f41e1b11a8876af27557b
Source noteuspto-grants-1997_06