Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975298Generated: October 30, 2026

4-Toluenesulfonyl chloride → Methyl 2-(4'-p-toluenesulfonyloxymethylphenyl)benzoate

https://huagongshe.com/reaction/975298

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
ReactantMethyl 4'-(hydroxymethyl)-[1,1'-biphenyl]-2-carboxylateHCID 15380881—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 2-(4'-p-toluenesulfonyloxymethylphenyl)benzoateHCID 1538088382.4%

Reaction Steps

10.0 g (41 mmol) of methyl 2-(4'-hydroxymethylphenyl)benzoate was dissolved in tetrahydrofuran (200 ml). 2.0 g (50 mmol) of a 60% sodium hydride was added thereto under cooling with ice, followed by stirring for one hour. A solution of 8.65 g (45.4 mmol) of p-toluenesulfonyl chloride in tetrahydrofuran (50 ml) was dropwise added thereto. Then, the reaction was effected at room temperature for 2 hours and further reflux by heating was effected for 4 hours. The reaction liquid was cooled and added to a saturated aqueous solution of ammonium chloride. The resulting mixture was extracted with chloroform (200 ml). After the organic phase was washed with water and dried, it was subjected to vacuum concentration. The residue was purified by silica gel column chromatography (a n-hexane/ethyl acetate system) to give 13.4 g of the title compound as a wax (yield 82%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05608068
Source datasetuspto-grants-1997_03
ORD IDord-065ded1481fa488ab21dfc84933ba11d
Source noteuspto-grants-1997_03