HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-(p-Fluorobenzoyl)-3-methoxycrotononitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Trimethyl orthoacetate | HCID 15050 | — |
| Reactant | p-Fluorobenzoylacetonitrile | HCID 2783172 | — |
| Product | 2-(p-Fluorobenzoyl)-3-methoxycrotononitrile | HCID 23468508 | — |
Reaction Steps
A solution containing 55.8 g. (0.34 mole) of p-fluorobenzoylacetonitrile, 41 g. (0.34 mole) of trimethyl orthoacetate, and 90 g. (0.88 mole) of acetic anhydride is heated to reflux for 5 hours. The excess solvent and volatile by-products are then removed by vacuum distillation and the residue is recrystallized from diethyl ether. Alternatively, the distillation residue may be distilled over on a Kugelrohr apparatus at 160° C./0.25 mm. to provide a viscous oil which may be crystallized from diethyl ether to provide the pure title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04259256 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-717749a389014f1390c6bee092a2ee54 |
| Source note | uspto-grants-1981_03 |