HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266591Generated: October 30, 2026
Acetic Acid → 4-(N,N-dimethylsulphamoyl)-2-trifluoromethylbenzoic acid
https://huagongshe.com/reaction/266591
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | HCID 54168288 | HCID 54168288 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(N,N-dimethylsulphamoyl)-2-trifluoromethylbenzoic acid | HCID 54115067 | — |
Reaction Steps
A mixture of 4-(N,N-dimethylsulphamoyl)-2-trifluoromethylbenzamide (1.38 g), acetic acid (10 ml) and concentrated sulphuric acid (0.5 ml) were heated to 70° C. and isoamyl nitrite (15 ml) was added over 4 hours. After cooling the mixture was poured into water and extracted with ethyl acetate and washed with water. The organic phase was extracted with 2M sodium carbonate and the aqueous layer acidified to pH 1 with 2M HCl. This was extracted with ethyl acetate, washed with water, dried (anhydrous magnesium sulphate) and filtered. The filtrate was evaporated to dryness and the residue passed through a short silica column eluting with dichloromethane-ethyl acetate to give 4-(N,N-dimethylsulphamoyl)-2-trifluoromethylbenzoic acid (0.98 g) as a white solid, m.p. 188.8°-189.4° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05650533 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-36572f42a4e246f7a2fee2369c55acd2 |
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| Source note | uspto-grants-1997_07 |
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