Phthalic Anhydride → HCID 11769653, compound
Reaction equation
[C:1]1(=[O:11])[O:6][C:4](=[O:5])[C:3]2=[CH:7][CH:8]=[CH:9][CH:10]=[C:2]12.[CH2:12]([OH:15])[CH:13]=[CH2:14]>>[CH2:12]([O:15][C:4](=[O:5])[C:3]1[C:2](=[CH:10][CH:9]=[CH:8][CH:7]=1)[C:1]([OH:6])=[O:11])[CH:13]=[CH2:14]Participants
3
Conditions
- Temperature
- 90 °C
Procedure
A 100-mL three-necked round-bottom flask was fitted with a reflux condenser and, in a nitrogen atmosphere, the flask was charged with phthalic anhydride (4.0 g, 13.5 mmol) and allyl alcohol (4.58 mL), and the contents were stirred at 90° C. for 30 minutes. The unreacted allyl alcohol fraction was distilled off under reduced pressure to give phthalic acid monoallyl ester (yield 5.66 g).
Workup
- customA 100-mL three-necked round-bottom flask was fitted with a reflux condenser and, in a nitrogen atmosphere
- distillationThe unreacted allyl alcohol fraction was distilled off under reduced pressure
Sources & evidence
- ORD record
- ord-1f9ebddba34842df96bf24959a4f304f
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06653429B1
Reaction notes
Loading…