Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1699479Generated: October 31, 2026

Benzenesulfonyl chloride → HCID 10924734, compound

https://huagongshe.com/reaction/1699479

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantPropargyl bromideHCID 7842—
ReactantTriethylamineHCID 8471—
Reactant4-MercaptophenolHCID 240147—
SolventEthyl AcetateHCID 8857—
ProductHCID 10924734HCID 10924734109.6%

Reaction Steps

4-Mercaptophenol (1) (37.85 g, 300 mmol) and propargyl bromide (42.82 g, 360 mmol) were dissolved in ethyl acetate (757 ml). To the solution was added dropwise triethylamine (42.5 g, 420 mmol) over 25 minutes with stirring and under ice-cooling. After stirring for another 1.5 hours at the same temperature, triethylamine (42.5 g, 420 mmol) was added in one portion, and benzenesulfonyl chloride (63.58 g, 360 mmol) was added dropwise over 20 minutes. After keeping 1 hour at the same temperature, the cooling bath was removed and the mixture was stirred for 30 minutes at room temperature and partitioned into two layers by adding ice-water (500 ml) and 2N hydrochloric acid (110 ml). The aqueous layer was extracted with ethyl acetate (200 ml). The combined organic layer was washed with water, dried over anhydrous magnesium sulfate, and then the solvent was distilled off under reduced pressure to provide 100.04 g of the title compound (2) as oil. Crude yield: 109%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06346628B1
Source datasetuspto-grants-2002_02
ORD IDord-188d2f78bb3544e2ae9af02df83b92e8
Source noteuspto-grants-2002_02