HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639192Generated: October 31, 2026
Acetic Acid → 4-Bromo-3,5-difluorobenzonitrile
https://huagongshe.com/reaction/1639192
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 4-Amino-3,5-difluorobenzonitrile | HCID 280467 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Product | 4-Bromo-3,5-difluorobenzonitrile | HCID 14794290 | — |
Reaction Steps
4 g of sodium nitride was added to 30 ml of concentrated sulfuric acid and chilled to a temperature of 10° C. and 38 ml of acetic acid was added thereto. 8.9 ml of 4-cyano-2,6-difluoroaniline was added gradually to maintain the solution at a temperature of 20° to 25° C. The reaction mixture was added dropwise to a solution a 10 g of copper (I) bromide dissolved in 30 ml of concentrated hydrobromic acid. After the dropwise addition was completed, the reaction mixture was stirred for one and one half hours at room temperature. Water was added to the reaction mixture, the reaction mixture was extracted with chloroform and washed with water. The organic layer was removed by distillation, and the residue was recrystallized with a mixture of methanol and acetone to yield 6.6 g of 2-bromo-5-cyano-1,3-difluorobenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04883609 |
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| Source dataset | uspto-grants-1989_11 |
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| ORD ID | ord-c518c4b4842a41ac80315e38abcc318d |
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| Source note | uspto-grants-1989_11 |
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