HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Cyanide → 2-(5-Bromo-2-fluorophenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 4-Bromo-2-(bromomethyl)-1-fluorobenzene | HCID 13553295 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(5-Bromo-2-fluorophenyl)acetonitrile | HCID 23509631 | — |
Reaction Steps
5-Bromo-2-fluorobenzyl bromide (8.0 g, 0.03 mole) was dissolved in 1,4-Dioxane (60 mL) and added to a solution of KCN (2.04 g, 0.031 mole) in H2O (20 mL) and ethanol ( 20 mL). The resulting mixture was heated under reflux for 5 h. After cooling to rt, the product was extracted with ether ( 200 mL), washed with brine, dried over MgSO4, concentrated. Crystallized from ether/hexane to give 5-bromo-2-fluorophenylacetonitrile as a white crystalline material (5.6 g, 88%): rp 55-58° C.; 1H NMR (DMSO-d6) □ 4.07 (s, 2H), 7.29( t, 1H,J=9.23 Hz), 7.60-7.69( m, 2H); MS(EI) M+ m/z 213 ; Anal. Calc. For C8H5Br2FN: C, 44.89, H, 2.35, N, 6.54. Found: C, 44.90, H, 2.24, N, 6.43.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06444668B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-5c35319bd86440b38b5c85c6f234a165 |
| Source note | uspto-grants-2002_09 |