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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953129Generated: November 2, 2026

Hydrochloric Acid → Methyl 2-amino-4-methanesulfonylbenzoate

https://huagongshe.com/reaction/1953129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 22621045HCID 22621045—
SolventMethanolHCID 887—
ProductMethyl 2-amino-4-methanesulfonylbenzoateHCID 2262094120.4%

Reaction Steps

Concentrated hydrochloric acid (90 ml) was added to a stirred suspension of methyl 2-nitro-4-methylsulphonylbenzoate (25 g) in methanol at -5° C. (ice/salt bath). The cooling bath was then removed and iron dust (17.5 g) was added portionwise over a period of 20 minutes. The resulting exotherm was controlled using a cooling bath so that the temperature did not exceed 50° C. After 15 minutes of cooling, the bath was removed and the reaction mixture was allowed to reach room temperature. Stirring was continued for a further 3 hours. The mixture was poured onto ice and then neutralised with sodium carbonate. Dichloromethane was added and the suspension was filtered. The filtrate was extracted with further dichloromethane and the combined organic extracts were dried (magnesium sulphate), filtered and evaporated to yield a crude product which was purified by recrystallisation from ethyl acetate/hexane to give methyl 2-amino4methylsulphonylbenzoate (4.5 g) as yellow needles, m.p. 98.3-98.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114538
Source datasetuspto-grants-2000_09
ORD IDord-6a5e77da51e643ebbf566701bc7cd2f1
Source noteuspto-grants-2000_09