HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287717Generated: October 26, 2026
Hydrochloric Acid → 3-Nitro-5-sulphamyl-4-(m-trifluoromethylphenoxy)-benzoic acid
https://huagongshe.com/reaction/1287717
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-(Trifluoromethyl)phenol | HCID 7376 | — |
| Reactant | 4-Chloro-3-nitro-5-sulphamoylbenzoic acid | HCID 89893 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 3-Nitro-5-sulphamyl-4-(m-trifluoromethylphenoxy)-benzoic acid | HCID 21312153 | — |
Reaction Steps
A mixture of 4-chloro-3-nitro-5-sulphamyl-benzoic acid (7 g), m-trifluoromethylphenol (20 g), and 1N sodium bicarbonate (100 ml) was stirred at 95° C for 6 hours. Then the reaction mixture was acidified by the addition of 4N hydrochloric acid and the excess of trifluoromethylphenol was removed by steam distillation. After cooling, the precipitated 3-nitro-5-sulphamyl-4-(m-trifluoromethylphenoxy)-benzoic acid was collected by suction and recrystallized several times from methanol-water. The melting point of the pure compound was 205°-206° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03985777 |
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| Source dataset | uspto-grants-1976_10 |
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| ORD ID | ord-b9536b1eceea461d8d566f5898cecd27 |
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| Source note | uspto-grants-1976_10 |
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