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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266263Generated: October 29, 2026

Acetone → HCID 18323177, compound

https://huagongshe.com/reaction/266263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantBenzenesulfonyl chlorideHCID 7369—
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 10 0 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 phenylsulfonyl chloride (phenylthio chloride) and 10 ml of anhydrous THF is then run in. The mixture is then left to return to more 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 numberUS05650519
Source datasetuspto-grants-1997_07
ORD IDord-a2713ab3b43c44e496d4c376b7ace3fd
Source noteuspto-grants-1997_07