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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81089Generated: October 28, 2026

4-Toluenesulfonyl chloride → HCID 178427753, compound

https://huagongshe.com/reaction/81089

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
ReactantHCID 178520956HCID 178520956—
SolventDichloromethaneHCID 6344—
ProductHCID 178427753HCID 178427753—

Reaction Steps

4-Toluenesulfonyl chloride (742.5 g, 3.75 mol) was added to a solution of trans-cyclohexane-1,4-diyldimethanol (500 g, 4.17 mol) and Et3N (695 g, 5 mol) in DCM (6000 mL) at −20° C. The mixture was stirred at room temperature for 10 h and then quenched with water (10 L). The organic layer was separated, the aqueous layer was extracted with DCM (2×3 L), and the combined organic layer was dried over sodium sulfate, filtered, and concentrated in vacuo to give trans-4-(hydroxymethyl)cyclohexylmethyl 4-methylbenzenesulfonate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846657B2
Source datasetuspto-grants-2014_09
ORD IDord-897e2997e61b482ab4b057fb6d14e464
Source noteuspto-grants-2014_09