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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423274Generated: October 31, 2026

Benzenesulfonyl chloride, 2,4-dichloro- → HCID 59864884, compound

https://huagongshe.com/reaction/2423274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chloride, 2,4-dichloro-HCID 204419—
ReactantHCID 59864814HCID 59864814—
SolventPyridineHCID 1049—
ProductHCID 59864884HCID 59864884—

Reaction Steps

To a room temperature solution of 1.3 (2.22 g, 6.52 mmol) dissolved in pyridine (14 mL) was added 2,4-dichlorobenzenesulfonyl chloride (1.76 g, 7.17 mmol). The resulting red solution was stirred at room temperature for 30 min., after which time LC-MS indicated no 13 remained. The reaction solution was concentrated in vacuo on a rotary evaporator and the concentrate partitioned between ethyl acetate and saturated aqueous sodium bicarbonate solution. The organic separation was washed with water then brine. The organic extract was stirred over magnesium sulfate, filtered and the filtrate concentrated in vacuo on a rotary evaporator to afford an orange oil. The product was isolated by chromatography on silica gel, eluting with ethyl acetate/hexane gradient, to afford a faint yellow solid. LC-MS ESI (pos.) m/z: 549.0 (100%), 551.0 (68%), 550.0 (28%) (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960567B2
Source datasetuspto-grants-2011_06
ORD IDord-9e55d51c5bdc46a3ac1ff86d02dad235
Source noteuspto-grants-2011_06