HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 971862Generated: October 27, 2026
Sulfuric Acid → 4'-Iodo-3'-trifluoromethylisobutyranilide
https://huagongshe.com/reaction/971862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | N-[4-Amino-3-(trifluoromethyl)phenyl]-2-methylpropanamide | HCID 16776651 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4'-Iodo-3'-trifluoromethylisobutyranilide | HCID 21312290 | — |
Reaction Steps
To a solution of 23.0 g. of 4'-amino-3'-trifluoromethylisobutyranilide in 150 ml. of glacial acetic acid and 100 ml. of water, while maintaining the mixture temperature at 10°-20° C., slowly add 17 ml. of concentrated sulfuric acid, cool the resulting mixture to about 0° C. and slowly add 8.5 g. of sodium nitrite in 15 ml. of water maintaining the temperature of the reaction at about 0° C. for 30 minutes. Add 50 g. of potassium iodide in 150 ml. of water and stir the resulting mixture for 1 hour. Filter, water-wash and dissolve the precipitate in 200 ml. of ether and remove the iodine by washing with a 10% sodium sulfite solution. Dry, remove the solvent, and recrystallize from carbon tetrachloride, obtaining the compound of this example, m.p. 143°-145° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04161540 |
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| Source dataset | uspto-grants-1979_07 |
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| ORD ID | ord-1b85c19aa6c74ff2acb031a52757dc92 |
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| Source note | uspto-grants-1979_07 |
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