Acetic Anhydride → HCID 18403028, compound
Reaction equation
[NH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]([OH:13])=[O:12])[CH:9]=2)[C:4](=[O:14])[CH2:3][CH2:2]1.[C:15](OC(=O)C)(=[O:17])[CH3:16]>O>[C:15]([N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([C:11]([OH:13])=[O:12])[CH:9]=2)[C:4](=[O:14])[CH2:3][CH2:2]1)(=[O:17])[CH3:16]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5.0 g of 2,3-dihydro-4-quinolone-7-carboxylic acid and 22.5 g of acetic anhydride were heated to 100° C. for 1 hour. After cooling, water was added and the mixture was extracted with methylene chloride. The organic phase was dried and concentrated.
Workup
- temperatureAfter cooling
- extractionthe mixture was extracted with methylene chloride
- customThe organic phase was dried
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-ade763334d314f79ac1e1800b0803958
- Source dataset
- uspto-grants-2002_11
- Patent number
- US06479436B1
Reaction notes
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