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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 22621045 | HCID 22621045 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-amino-4-methanesulfonylbenzoate | HCID 22620941 | 20.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06114538 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-6a5e77da51e643ebbf566701bc7cd2f1 |
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| Source note | uspto-grants-2000_09 |
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