HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-(2-Fluorophenyl)propanenitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-(2-Fluorophenyl)ethan-1-ol | HCID 2733296 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-Fluorophenyl)propanenitrile | HCID 39058336 | — |
Reaction Steps
To a solution of 2-(2-fluoro-phenyl)-ethanol (10.00 g, 71.50 mmol) in CH2Cl2 at 0° C. was added Et3N (20.00 mL, 0.14 mol) followed by MsCl (19.00 mL, 0.25 mol). The resulting mixture was stirred for 1 hour, then washed with H2O (3×100 mL) and brine (1×150 mL), dried over MgSO4 and concentrated. The residue was dissolved in DMF and KCN (9.30 g, 0.14 mol) was added. The resulting mixture was stirred at 75° C. for 14 hours. After cooling to room temperature, the reaction mixture was quenched into water and extracted with Et2O (3×300 mL). The combined organic extracts were washed with H2O (2×200 mL), brine (1×200 mL), dried over MgSO4 and concentrated to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07884244B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-72d90371c0e1471db152b857f2e3023c |
| Source note | uspto-grants-2011_02 |