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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789458Generated: October 30, 2026

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

https://huagongshe.com/reaction/1789458

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 numberUS04689341
Source datasetuspto-grants-1987_08
ORD IDord-0dd86c3f04a44ab8bb79b472f6559150
Source noteuspto-grants-1987_08