Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463751Generated: October 29, 2026

4-Toluenesulfonyl chloride → HCID 178427750, compound

https://huagongshe.com/reaction/1463751

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantHCID 178520952HCID 178520952—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 178427750HCID 178427750—

Reaction Steps

A solution of 2.96 g of crude (trans-4-[trans-4-(2-(1,3-dioxolan-2-yl)ethyl)cyclohexyl]cyclohexyl ]methanol in 20 ml of dry pyridine is treated at 0° C. with 2.1 g of p-toluenesulfonyl chloride. The mixture is stirred at room temperature for 15 hours, then diluted with 200 ml of methylene chloride and washed several times with water. The organic phase is dried over magnesium sulfate, filtered and evaporated. Chromatographic purification of the resulting crude product on silica gel with ethyl acetate/petroleum ether (vol. 1:9) gives [trans-4-[trans-4-(2-(1,3-dioxolan-2-yl)ethyl ]cyclohexyl]cyclohexyl]methyl p-toluenesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05302317
Source datasetuspto-grants-1994_04
ORD IDord-6cb7365fa79841d09dab9b3637400c4f
Source noteuspto-grants-1994_04