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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2394932Generated: October 29, 2026

Water → 4-Nitrobenzenesulfonyl chloride

https://huagongshe.com/reaction/2394932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSulfuryl chlorideHCID 24648—
Reactant4-Nitrophenyl methyl sulfideHCID 96109—
SolventChlorobenzeneHCID 7964—
Product4-Nitrobenzenesulfonyl chlorideHCID 740495.2%

Reaction Conditions

Temperature10 °C

Reaction Steps

A 2-liter, 4-necked flask equipped with a stirrer, thermometer, condenser and a dropping funnel having a by-pass was charged with 20.4 g (0.10 mole) of 4-nitrophenyl methyl sulfide, 10 g of water and 200 g of monochlorobenzene. Then, 94.5 g (0.70 mole) of sulfuryl chloride was added dropwise at 10° C. over a period of about 2 hours. Thereafter the mixture was stirred at 10° C. for 6 hours to complete the reaction. After completion of the reaction, the oil layer was separated and 10 g of water was added to accomplish washing. Then, the oil layer was separated and left to stand for about 1 hour with the addition of about 5 g of anhydrous sodium sulfate to remove the water. The solvent was distilled off to give crude crystals. The crude crystals were dissolved in monochlorobenzene and a poor solvent was added for recrystallization, giving 21.1 g of 4-nitrobenzenesulfonyl chloride as white crystals in a yield of 95% as calculated based on 4-nitrophenyl methyl sulfide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05811571
Source datasetuspto-grants-1998_09
ORD IDord-5f236e35a596452fbd6e645cf373848e
Source noteuspto-grants-1998_09