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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380347Generated: October 31, 2026

4-Toluenesulfonyl chloride → (Z)-4-(4-Chlorophenyl)-2-buten-1-ol 4-methylbenzenesulfonate

https://huagongshe.com/reaction/1380347

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantPotassium HydroxideHCID 14797—
Reactant(Z)-1-(4-chlorophenyl)-2-buten-1-olHCID 67901371—
SolventDiethyl EtherHCID 3283—
Product(Z)-4-(4-Chlorophenyl)-2-buten-1-ol 4-methylbenzenesulfonateHCID 131714350—

Reaction Steps

Dissolve 6.7 g (0.036 mole) of (Z)-1-(4-chlorophenyl)-2-buten-1-ol in 100 ml of anhydrous ether, add 3.2 g of powdered KOH. Stir the mixture and with cooling add a solution of 7.0 g p-toluenesulfonylchloride in 30 ml of anhydrous ether. Continue to stir with cooling for 30 minutes, then allow to warm to room temperature overnight. Filter, wash the filtrate three times with saturated aqueous sodium bicarbonate, then with water and dry over sodium sulfate. Evaporate off solvents and triturate residue with petroleum ether, cyclohexane. Recrystallize residue from cyclohexane to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04581370
Source datasetuspto-grants-1986_04
ORD IDord-a365e688f69b4b698fb43abc0896a324
Source noteuspto-grants-1986_04