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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796404Generated: October 30, 2026

Acetone → HCID 21866714, compound

https://huagongshe.com/reaction/1796404

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantChlorobutanolHCID 5977—
ReactantSodium HydroxideHCID 14798—
ReactantHydrideHCID 166653—
ReactantHCID 21866825HCID 21866825—
SolventWaterHCID 962—
ProductHCID 21866714HCID 21866714—

Reaction Steps

Under argon atmosphere, 24 mg of triturated sodium hydroxide was added to 2 ml of a solution of 100 mg of 4-(6-acetylthiohexyl)-5-methyl-2-(p-tolyl)oxazole in acetone, and stirred for 2 hours at room temperature. To the reaction solution, 20 μl of water was added, followed by addition of 113 mg of 1,1,1-trichloro-2-methyl-2-propanol.0.5 hydride (chloretone), and then 96.5 mg of triturated sodium hydroxide in tree portions at 30 minutes intervals. The mixture was stirred for additional 18 hours at room temperature. The reaction solution was concentrated. The residue was, after addition of water, extracted with diethyl ether. The organic layers were combined, washed with water, and the washings was acidified with 1 N hydrochloric acid and extracted with ethyl acetate. The organic layers were combined, washed with water and brine sequentially, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (Wakogel® C-200, chloroform:methanol=100:1) and the resulting crystals were washed with n-hexane to provide 28.0 mg of the objective compound as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030143B2
Source datasetuspto-grants-2006_04
ORD IDord-677b7d951ebf4ea5a3345a215bae1f35
Source noteuspto-grants-2006_04