Acetic Anhydride → HCID 12227147, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[O:13][C:12]([CH:14]=[N:15]O)=[CH:11][CH:10]=2)=[CH:5][CH:4]=1.C(OC(=O)C)(=O)C>CCOCC>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[O:13][C:12]([C:14]#[N:15])=[CH:11][CH:10]=2)=[CH:5][CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 500 ml three-necked flask equipped with stirrer, thermometer and reflux condenser was charged with 5-(p-methoxyphenyl)-2-furaldehyde oxime (28 g, 0.129 mole) and acetic anhydride (317 ml). This mixture was refluxed (138°) for 3 hours. After cooling to room temperature overnight, the green solution was poured into ice water (ca. 2l. ) with stirring. When the ice melted, the solid was collected by filtration, washed with water, and dried to give 26 g.
Workup
- customA 500 ml three-necked flask equipped with stirrer
- temperaturethermometer and reflux condenser
- temperatureThis mixture was refluxed (138°) for 3 hours
- filtrationthe solid was collected by filtration
- washwashed with water
- customdried
- customto give 26 g
Sources & evidence
- ORD record
- ord-5326d26079af4b7ca96f8d30b084d4bc
- Source dataset
- uspto-grants-1976_03
- Patent number
- US03946049
Reaction notes
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