HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Cyanide → 2-(Trifluoromethoxy)phenylacetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | 2-(Trifluoromethoxy)benzyl bromide | HCID 2777254 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Trifluoromethoxy)phenylacetonitrile | HCID 2777321 | — |
Reaction Steps
To a stirred solution of 2-trifluoromethoxybenzyl bromide (0.95 g, 3.9 mmol) from Step 2 above in DMF (5 mL) was added NaCN (0.21 g, 4.3 mmol). The mixture was stirred at ambient temperature for 14 h and the solvent was removed under reduced pressure. The residue was purified by pressurized silica gel column chromatography using 15% EtOAc-hexanes as eluant to give 2-trifluoromethoxyphenylacetonitrile as a colorless liquid (TLC Rf =0.6 (solvent)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06090805 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-8f1d8a84fd2d4d6ebb75db4419a0f787 |
| Source note | uspto-grants-2000_07 |