HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2232650Generated: October 29, 2026
Benzene → 3-Bromo-2-chloro-4,5-difluorobenzonitrile
https://huagongshe.com/reaction/2232650
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Bromo-2-chloro-4,5-difluorobenzenediazonium tetrafluoroborate | HCID 14365253 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Bromo-2-chloro-4,5-difluorobenzonitrile | HCID 14071796 | 41.4% |
Reaction Steps
3-Bromo-2-chloro-4,5-difluorobenzenediazonium tetrafluoroborate (35.6 g) was added portionwise during 40 minutes to a solution of cuprous cyanide (18.67 g), potassium cyanide (27.14 g) and sodium carbonate (5.52 g) in water (200 ml) with stirring vigorously at room temperature. After the mixture was stirred for 4.5 hours, benzene (250 ml) was added to the suspension and then the mixture was stirred for 25 minutes. The insoluble materials were collected by filtration, and washed with benzene. The filtrate and washings were combined and washed with water, dried over anhydrous sodium sulfate and then concentrated. The resulting residue was purified by silica gel chromatography eluting with dichloromethane-n-hexane (1:3) and further recrystallized from n-hexane-dichloromethane to give the title compound (10.9 g) as light yellow needles, mp 71°-72.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04788320 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-8dfe79a4c4b2492082cbdb6da922054e |
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| Source note | uspto-grants-1988_11 |
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