HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453069Generated: October 30, 2026
Potassium Cyanide → 2-(4-Bromo-2-fluorophenyl)acetonitrile
https://huagongshe.com/reaction/1453069
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4-Bromo-2-fluorobenzyl bromide | HCID 2733660 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(4-Bromo-2-fluorophenyl)acetonitrile | HCID 7172308 | 87.4% |
Reaction Steps
To a solution of 4-bromo-1-(bromomethyl)-2-fluorobenzene (5.0 g, 18.7 mmol) in DMF (80 mL) and H2O (8 mL) was added KCN (1.21 g, 18.7 mmol). The mixture was heated to 40° C. for 3 hours before it was cooled down to room temperature. The reaction was diluted with H2O (40 mL) and extracted with Et2O (3×100 mL). The combined organic layers were washed with brine and dried over Na2SO4. The solvent was removed and the residue was purified by flash column chromatography (0-15% EtOAc in hexanes) to give the product (3.5 g, 87% yield). 1H NMR (300 MHz, CDCl3) δ: 3.72 (s, 2H), 7.26-7.35 (m, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07473790B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-ee48cd856c744c1aa34ec7427d49f1f1 |
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| Source note | uspto-grants-2009_01 |
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