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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 236084Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 20217759, compound

https://huagongshe.com/reaction/236084

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactantp-ChlorothiophenolHCID 7815—
ReactantSodium CarbonateHCID 10340—
ReactantPiperidin-2-ylmethanolHCID 94263—
SolventPyridineHCID 1049—
SolventDimethylformamideHCID 6228—
SolventSodium HydroxideHCID 14798—
ProductHCID 20217759HCID 20217759—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 57.92 g (0.504 mole) of 2-hydroxymethylpiperidine and 236 g (1.24 mole) of tosychloride in one liter of pyridine was stirred at 25° C. overnight. The mixture was quenched in water and the aqueous mixture was extracted with several portions of methylene chloride. The combined methylene chloride extract was extracted with 1M sulfuric acid solution followed by 1M aqueous sodium hydroxide, dried over magnesium sulfate and evaporated to give an oil which was shown by NMR and mass spectrometry to be 1-[(4-methylphenyl)sullfonyl[-2-piperidinemethanol ester with 4-methylbenzene sulfonic acid. A mixture of 40.78 g (0.0964 mole) of the oil, 24.60 g (0.171 mole) of p-chlorothiophenol and 25.4 g of sodium carbonate in 200 ml of dimethylformamide was stirred at 100° C. overnight and then quenced in dilute sodium hydroxide. The mixture was extracted with several portions of methylene chloride. The combined extract was extracted with several portions of 1M sodium hydroxide, dried over magnesium sulfate and evaporated in vacuo to give an oil. The oil was crystallized from ether-hexane to give 29.73 g of the solid product. On standing at room temperature, the solid melted.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04642348
Source datasetuspto-grants-1987_02
ORD IDord-d042453a59e24b4d8d0c1fc22a20a8f7
Source noteuspto-grants-1987_02