HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1707522Generated: October 30, 2026
Acetic Acid → 4-Bromo-3,5-difluorobenzonitrile
https://huagongshe.com/reaction/1707522
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Amino-3,5-difluorobenzonitrile | HCID 280467 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Product | 4-Bromo-3,5-difluorobenzonitrile | HCID 14794290 | — |
Reaction Steps
While stirring 420 cm3 of concentrated H2SO4 on an ice water bath, 54 g (0.78 mol) of pulverized NaNO2 was added at a rate that maintained a temperature under 40° C., and after the addition it was stirred in a hot water bath at 50° C. until the crystals dissolved completely. While stirring this solution on an ice water bath, 700 cm3 of glacial acetic acid was added dropwise, then 108 g (0.7 mol) of 4-amino-3,5-difluorobenzonitrile was added at a rate maintaining the temperature at 20°-25° C., and after the addition was completed it was stirred at this temperature until the crystals were completely dissolved to prepare a diazonium salt solution. A solution with 143 g (1.0 mol) of CuBr dissolved in 420 cm3 of 47% HBr was stirred in an ice water bath while the previously prepared diazonium salt solution was added dropwise for 2 hours, and after the dropping was completed, it was stirred on an ice water bath for 1 hour and at room temperature overnight. The crystals formed were filtered, and after washing the crystals in glacial acetic acid, they were recrystallized from a mixture of acetone and methanol to obtain 98 g (0.44 mol) of 4-bromo-3,5-difluorobenzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05354502 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-80f863b243ce4abd909dc447ef412891 |
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| Source note | uspto-grants-1994_10 |
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