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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437612Generated: October 30, 2026

Acetone → 2,2,6-Trimethyl-1,3-oxathiane

https://huagongshe.com/reaction/437612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantDiethylamineHCID 8021—
Reactant1-mercaptobutan-3-olHCID 3703445—
SolventDichloromethaneHCID 6344—
Product2,2,6-Trimethyl-1,3-oxathianeHCID 547827—

Reaction Steps

75 ml of dichloromethane is placed into a 100 ml round-bottom flask. To the dichloromethane is added 5.3 grams (0.05 moles) of 4-mercapto-2-butanol. 3.2 grams (0.055 moles) of acetone is then added followed by 0.1 grams of p-toluene sulfonic acid. Boiling chips are added to the flask. A Dean-Starke distilling receiver is placed on the flask, and a reflux condenser is placed on the receiver. The flask is then heated slowly until reflux occurs, and then the temperature is increased for a more vigorous reflux. The reflux lasts for a period of 2 hours before water of reaction ceases to be formed. The reaction mass is then cooled and neutralized with diethyl amine to a pH of about 8. The reaction mass is filtered through fluted filter paper, and the dichloromethane solvent is removed by means of rotary evaporation. 7.2 grams of crude product are recovered after the rotary evaporation operation. The crude product is then distilled by means of vacuum distillation yielding the following 3 fractions:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031257
Source datasetuspto-grants-1977_06
ORD IDord-5d711e075d7f419795a23d11f6b6a165
Source noteuspto-grants-1977_06