HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-[4-(4-Fluorophenyl)oxan-4-yl]acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 68314247 | HCID 68314247 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 2-[4-(4-Fluorophenyl)oxan-4-yl]acetonitrile | HCID 68314336 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
To a pre-dissolved solution of KOH (441 mg, 7.87 mmol) in ethylene glycol (20 ml) was added methyl 2-cyano-2-[4-(4-fluorophenyl)oxan-4-yl]acetate (1.09 g, 3.93 mmol). The mixture was heated to 120° C. for 3 h, and then cooled. H2O was added (50 ml), the product extracted with Et2O (3×50 ml), washed with H2O (50 ml), dried over NA2SO4, filtered and concentrated. Purified by normal phase SiO2 chromatography (5 to 40% EtOAc/hexanes) to give 2-[4-(4-fluorophenyl)oxan-4-yl]acetonitrile as a colorless oil (450 mg, 78%, m/z: 219.1 [M+H]+ observed).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09044469B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-6e04ebacc15b4e438e419dc49931b4f5 |
| Source note | uspto-grants-2015_06 |