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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437614Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 21417756, compound

https://huagongshe.com/reaction/437614

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAcetophenoneHCID 7410—
ReactantSodium BicarbonateHCID 516892—
Reactant1-mercaptobutan-3-olHCID 3703445—
SolventDichloromethaneHCID 6344—
ProductHCID 21417756HCID 21417756—

Reaction Steps

74 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. 6.6 grams (0.055 moles) of acetophenone 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 refluxing lasts for a period of 3 hours before water of reaction ceases to be formed. The reaction mass is then cooled and neutralized with 10% aqueous sodium bicarbonate to a pH of 8. The reaction mass is filtered through fluted filter paper, and the dichloromethane solvent is removed by means of rotary evaporation. 10.4 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-907d4cf333f74c619a2f4bc6811751c8
Source noteuspto-grants-1977_06