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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607253Generated: October 30, 2026

Benzenesulfonyl chloride, 4-chloro-3-nitro- → HCID 5016179, compound

https://huagongshe.com/reaction/607253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chloride, 4-chloro-3-nitro-HCID 7323—
Reactant4-BromoanilineHCID 7807—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
ProductHCID 5016179HCID 501617952%

Reaction Steps

A solution of 4-chloro-3-nitrobenzenesulfonyl chloride (2.561 g, 10 mmol) in acetic acid (20 mL) was treated with 4-bromoaniline (1.72 g, 10 mmol) and anhydrous sodium acetate (1.23 g, 15 mmol), then heated at 100° for 30 minutes. The reaction was cooled to room temperature and the acetic acid removed by rotary evaporation under vacuum. The residue was taken up in ethyl acetate (100 mL) and washed with water (2×25 mL) and brine (25 mL). The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum, co-evaporating the oil with methylene chloride/hexanes. Purification by silica gel chromatography using methylene chloride followed by 5% ethyl acetate/methylene chloride as eluent provided the title compound as a yellow solid (2.038 g, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915411B2
Source datasetuspto-grants-2011_03
ORD IDord-12f0b37fc3244b058dd384cb112d8fc0
Source noteuspto-grants-2011_03