HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 382380Generated: October 31, 2026
Methylamine → 4-(Methylsulfamoyl)benzoic acid
https://huagongshe.com/reaction/382380
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Chlorosulfonyl)benzoic acid | HCID 82385 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Methylsulfamoyl)benzoic acid | HCID 506056 | 67.4% |
Reaction Steps
2.8 ml (20 mmol) triethylamine was added to and dissolved in a suspension of 4.4 g (20 mmol) of 4-chlorosulfonylbenzoic acid in dichloromethane. To the solution 3.1 ml of 40% aqueous solution of methylamine was added and stirred at room temperature overnight. After the reaction solution was concentrated under vacuum, the residue was dissolved in ethyl acetate-5% sodium hydrogencarbonate aqueous solution. The water layer was washed with ethyl acetate and adjusted to 2-3 pH with citric acid. The organic layer obtained by extracting the water layer with ethyl acetate was washed with distilled water, then with saturated brine, dried over anhydrous magnesium sulfate. This solution was concentrated under vacuum and the residue was crystallized from ethyl acetate-hexane to obtain 2.9 g of 4-methylaminosulfonylbenzoic acid (yield 67%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06310070B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-3e351e79393a41bb9556d0f37243d886 |
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| Source note | uspto-grants-2001_10 |
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