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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441775Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 21417750, compound

https://huagongshe.com/reaction/441775

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantDecanalHCID 8175—
ReactantSodium BicarbonateHCID 516892—
Reactant1-mercaptobutan-3-olHCID 3703445—
SolventDichloromethaneHCID 6344—
ProductHCID 21417750HCID 21417750—

Reaction Steps

75 ml of dichloromethane is placed in a 100 ml round-bottom flask. To the dichloromethane is added 5.3 grams (0.05 moles) of 4-mercapto-2-butanol. 8.58 grams (0.055 moles) n-decanal 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 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. 11.8 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 4 fractions:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04042601
Source datasetuspto-grants-1977_08
ORD IDord-977c4fac501041ee85b5e567eefc7f6f
Source noteuspto-grants-1977_08