HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 995Generated: October 23, 2026
Methanol → 2-Methoxycarbonyl-5-nitrobenzenesulfonic acid
https://huagongshe.com/en/reaction/995
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Nitro-2-sulfobenzoic acid | HCID 407025 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Methoxycarbonyl-5-nitrobenzenesulfonic acid | HCID 19693801 | — |
Reaction Steps
A suspension of 190.0 g (0.77 mol) of 2-carboxy-5-nitrobenzenesulfonic acid, 10 ml of DMF and 250 ml (3.43 mol) of thionyl chloride is heated at boiling for 3 h. After separating off the insoluble constituents by filtration, the filtrate is concentrated. 200 ml (4.94 mol) of methanol are added to the residue which results. When addition is complete the reaction mixture is cooled to 0° C. The solid which precipitates is filtered off and dried. 70.9 g (35.3% of theory) of colorless, crystalline 2-methoxycarbonyl-5-nitrobenzenesulfonic acid (m.p.: 92°-94° C.) are thus obtained. By distilling off the volatile components from the mother liquor, a second fraction (62.5 g, 31.1% of theory) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05723409 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-ef5dd0a2d9f54429bb4780c2b3d7888b |
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| Source note | uspto-grants-1998_03 |
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