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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341753Generated: October 26, 2026

Ammonium Chloride → 3-(Methylsulphonyl)aniline

https://huagongshe.com/reaction/341753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(Methylsulfonyl)-3-nitrobenzeneHCID 76312—
SolventWater ethanolHCID 19096565—
Product3-(Methylsulphonyl)anilineHCID 42802985.5%

Reaction Steps

(3-Nitro)phenyl methyl sulphone (prepared as described in Step 1 above) (5.396 g) reduced iron (7.5 g) and ammonium chloride (7.18 g) were mixed together in ethanol/water (2:1) (150 ml) and heated under reflux for 2 hours. The black solution was filtered through `Celite` and the pad washed with ethyl acetate. The solvents were removed under reduced pressure and the residue taken up in ethyl acetate/water. The organic layer was separated and the aqueous layer extracted with 3 further portions of ethyl acetate. The combined organic layers were washed with brine and the solvent removed under reduced pressure to give a dark orange oil (3.9275 g). This was chromatographed on silica gel using ethyl acetate-hexane (45:55 to 50:50) as eluant to give the title compound as an orange oil, yield 3.607 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05856273
Source datasetuspto-grants-1999_01
ORD IDord-468b3da800a94e858c6b6de404755328
Source noteuspto-grants-1999_01