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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482447Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 18981105, compound

https://huagongshe.com/reaction/482447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 18981120HCID 18981120—
SolventPyridineHCID 1049—
ProductHCID 18981105HCID 18981105—

Reaction Steps

Benzenesulfonyl chloride (0.57 ml) was slowly added dropwise at 0° C. to 10 ml of pyridine containing 1.5 g of the compound obtained in Example 66. The mixture was stirred at room temperature for 12 hours. After adding a saturated sodium bicarbonate solution, the reaction mixture was extracted with dichloromethane. The organic layer was washed with diluted hydrochloric acid, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from diethyl ether to give 1.75 g of the desired compound as colorless crystals. Table 3 shows the chemical structure and physical property (melting point) of the compound obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05798344
Source datasetuspto-grants-1998_08
ORD IDord-98637decdb4b49b6862df092579e1d0c
Source noteuspto-grants-1998_08