Acetic Anhydride → HCID 13017506, compound
Reaction equation
[CH3:1][C:2]1[C:11]([C:12](O)=[O:13])=[C:10]([C:15]([OH:17])=[O:16])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH3:18])[CH:8]=2)[N:3]=1.C(OC(=O)C)(=O)C>>[CH3:1][C:2]1[C:11]2[C:12]([O:16][C:15](=[O:17])[C:10]=2[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH3:18])[CH:8]=2)[N:3]=1)=[O:13]Participants
3
Procedure
A 2 L round bottom flask fitted with a magnetic stirring bar, reflux condenser, and drying tube was charged with 70 g (0.285 mole) of (i) and 1 L of reagent grade acetic anhydride. The tan suspension was stirred at reflux for 23 hours.
Workup
- customA 2 L round bottom flask fitted with a magnetic stirring bar
- temperaturereflux condenser
- customdrying tube
- temperatureat reflux for 23 hours
Sources & evidence
- ORD record
- ord-1e892f2fcfc74db0b04f7d0ad31d4319
- Source dataset
- uspto-grants-1984_04
- Patent number
- US04440768
Reaction notes
Loading…