Hydrochloric Acid → HCID 21559722, compound
Reaction equation
C([O:4][C:5]1[CH:18]=[CH:17][C:8]2[C:9](=[O:16])[C:10]([C:14]#[N:15])=[C:11]([CH3:13])[O:12][C:7]=2[CH:6]=1)(=O)C.[OH-].[Na+].Cl>CO>[OH:4][C:5]1[CH:18]=[CH:17][C:8]2[C:9](=[O:16])[C:10]([C:14]#[N:15])=[C:11]([CH3:13])[O:12][C:7]=2[CH:6]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A slurry of 7.3 g of 7-acetoxy-4-oxo-2-methyl-4H-1-benzopyran-3-carbonitrile in 45 ml of methanol was treated with 75 ml of 1N sodium hydroxide solution. The mixture was stirred for 5 minutes, cooled in ice and acidified with 4N HCl. The solid was filtered and recrystallized from methanol, mp > 300° C.
Workup
- temperaturecooled in ice
- filtrationThe solid was filtered
- customrecrystallized from methanol, mp > 300° C.
Sources & evidence
- ORD record
- ord-317f4dee3a6443e6b0515b6bc1f6c248
- Source dataset
- uspto-grants-1976_02
- Patent number
- US03937837
Reaction notes
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