HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981062Generated: November 1, 2026
Acetic Acid → 2-Hydroxy-5-sulfamoylbenzoic acid
https://huagongshe.com/reaction/981062
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 2-Methoxy-5-sulfamoylbenzoic acid | HCID 89601 | — |
| Solvent | Ethylacetate methanol | HCID 21584119 | — |
| Product | 2-Hydroxy-5-sulfamoylbenzoic acid | HCID 7731270 | — |
Reaction Steps
A mixture of 2-methoxy-5-sulfamoylbenzoic acid (58 g, 0.25 mole), 48% hydrobromic acid (150 ml), and acetic acid (150 ml) was heated to reflux for five hours. The progress of reaction was checked by thin layer chromatography (silica gel, 7:2:1 ethylacetate/methanol/29% ammonium hydroxide). Upon cooling, a solid crystallized out which was collected by filtration, and rinsed with cold water. This solid was dissolved in hot water (≤85° C.) and filtered through Celite® and recrystallized from the cool filtrate. Some of the recrystallized material was crystallized once more by dissolving in methanol, filtering, and mixing with excess amount of 1,1,1-trichloroethane. The mixture was evaporated to remove most of the methanol, and the resulting crystallizing mixture was stirred in ice bath. The solid was collected by filtration and rinsed with 1,1,1-trichloroethane, vacuum pumped at room temperature overnight to give a white solid, mp 234°-235° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04990523 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-4592699936f64f34a2d1a8a5adf9fa76 |
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| Source note | uspto-grants-1991_02 |
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