HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-(1,3-Benzoxazol-2-yl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2-Aminophenol | HCID 5801 | — |
| Reactant | 2-Hydroxybutanedinitrile | HCID 21253562 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(1,3-Benzoxazol-2-yl)acetonitrile | HCID 843325 | 71.8% |
Reaction Steps
To a solution of 2-aminophenol (5.0 g, 45.8 mmol) dissolved in 115 mL of anhydrous ethanol and 8 mL of glacial acetic acid was added malonitrile (9.08 g, 140 mmol) at 100° C. The resulting homogeneous solution was refluxed for 24 hours and the solvent was removed in vacuo to yield a red/brown oil. The oil was diluted with CH2Cl2 (100 mL) and any remaining solids were then removed by filtration. The mother liquor was washed twice with a saturated sodium bicarbonate solution and twice with water, dried over magnesium sulfate, filtered and evaporated to yield 5.2 g (71%) of the product as a yellow oil. This material was used in the subsequent reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08754233B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-e354f1356db7470fb5c54e9866d65951 |
| Source note | uspto-grants-2014_06 |