HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280503Generated: October 29, 2026
p-Toluenesulfonic acid → Cyclohexyl 3-sulfanylpropanoate
https://huagongshe.com/reaction/280503
Participants
| Role | Name | HCID | Charge |
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| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 3-Mercaptopropionic Acid | HCID 6514 | — |
| Reactant | Cyclohexanol | HCID 7966 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Cyclohexyl 3-sulfanylpropanoate | HCID 13651838 | — |
Reaction Steps
Into a 250 ml reaction flask equipped with stirrer, thermometer, reflux condenser and heating mantle are placed 100 grams of cyclohexanol; 26 grams of 3-mercaptopropionic acid and 0.5 grams of paratoluene sulfonic acid. The reaction mass is heated to reflux and refluxed for a period of 11 hours. At the end of the 11 hour period of refluxing, the reaction mass is cooled to room temperature. 200 ml Diethylether are added to the reaction mass. The reaction mass is then washed with two 100 ml volumes of 10% aqueous sodium bicarbonate solution followed by one 100 ml volume of water. The reaction mass is dried over anhydrous sodium sulfate and the solvent is recovered on a Buchi evaportor. The reaction mass is then micro distilled on a micro distillation apparatus yielding the following fractions:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04590082 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-fbb8db47f2114ff093fcc83db450cbfd |
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| Source note | uspto-grants-1986_05 |
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