Sodium Hydroxide → HCID 13543942, compound
Reaction equation
[O:1]=[C:2]1[C:7]2[CH:8]=[C:9]3[C:14](=[C:15]([CH2:16][CH2:17][CH3:18])[C:6]=2[O:5][C:4]([C:24]([O:26]CC)=[O:25])=[CH:3]1)[N:13]=[C:12]([C:19]([O:21]CC)=[O:20])[CH:11]=[CH:10]3.[OH-].[Na+]>CO>[O:1]=[C:2]1[C:7]2[CH:8]=[C:9]3[C:14](=[C:15]([CH2:16][CH2:17][CH3:18])[C:6]=2[O:5][C:4]([C:24]([OH:26])=[O:25])=[CH:3]1)[N:13]=[C:12]([C:19]([OH:21])=[O:20])[CH:11]=[CH:10]3Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product of step (b) (1.118 g) was suspended in methanol (100 mls) and heated and stirred under reflux with the dropwise addition of N/10 sodium hydroxide solution (58.37 mls). The reaction mixture was stirred and heated under reflux for a further 15 mins, cooled, filtered and acidified. The precipitated product was collected by filtration, washed with water and dried to give 0.852 g, mp 252° dec.
Workup
- temperatureheated
- stirringThe reaction mixture was stirred
- temperatureheated
- temperatureunder reflux for a further 15 mins
- temperaturecooled
- filtrationfiltered
- filtrationThe precipitated product was collected by filtration
- washwashed with water
- customdried
- customto give 0.852 g, mp 252° dec.
Sources & evidence
- ORD record
- ord-913ed98eea6e48a5a90330a29d1e0902
- Source dataset
- uspto-grants-1983_12
- Patent number
- US04419352
Reaction notes
Loading…