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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1268112Generated: October 31, 2026

Thionyl Chloride → HCID 12041317, compound

https://huagongshe.com/reaction/1268112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant2-AminobenzenesulfonamideHCID 72894—
ReactantHCID 8706988HCID 8706988—
SolventBenzeneHCID 241—
ProductHCID 12041317HCID 1204131787%

Reaction Steps

A benzene (20 ml) solution containing 1.40 (5.1 mmol) of 3-(4-nitrobenzyloxy)benzoic acid and 2 ml of thionyl chloride was heated under reflux for 2 hours and then the solvent was evaporated under a reduced pressure. The resulting residue was dissolved in methylene chloride (20 ml), this solution was added dropwise under ice-cooling to a pyridine (30 ml) solution containing 0.97 g (5.6 mmol) of 2-aminobenzenesulfonamide, the mixture was stirred at room temperature for 18 hours and then methylene chloride was evaporated under a reduced pressure. The resulting residue was dissolved in ethyl acetate, washed with a 1 N hydrochloric acid aqueous solution, water and saturated brine in that order and dried over anhydrous sodium sulfate, and then the solvent was evaporated under a reduced pressure. The thus obtained crude crystals were washed with methanol to obtain 1.9 g (yield: 87.0%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06555584B1
Source datasetuspto-grants-2003_04
ORD IDord-0d4a9a5ea1a8461ab75ada2082f92879
Source noteuspto-grants-2003_04