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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082021Generated: October 29, 2026

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

https://huagongshe.com/reaction/1082021

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodiumHCID 5360545—
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 hydrode 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 was (yield 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05587504
Source datasetuspto-grants-1996_12
ORD IDord-50ef8177ec3d4eabb301782df0b0374f
Source noteuspto-grants-1996_12