Acetic Acid → HCID 13067121, compound
Reaction equation
[Mn]([O-])(=O)(=O)=O.[K+].[Cl:7][C:8]1[CH:30]=[CH:29][C:11]2[C:12]3[C:13](=[C:24]([CH:27]=[O:28])[NH:25][CH:26]=3)[CH2:14][N:15]=[C:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[Cl:23])[C:10]=2[CH:9]=1.C(O)(=[O:33])C>CC(C)=O.S(=O)(O)[O-].[Na+]>[Cl:7][C:8]1[CH:30]=[CH:29][C:11]2[C:12]3[C:13](=[C:24]([C:27]([OH:33])=[O:28])[NH:25][CH:26]=3)[CH2:14][N:15]=[C:16]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[Cl:23])[C:10]=2[CH:9]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 1.5 g (9.5 mmol) of potassium permanganate in 150 ml of 50% aqueous acetone was added dropwise to a solution of 1.6 g (4.5 mmol) of 8-chloro-6-(2-chlorophenyl)-2H,4H-pyrrolo[3,4-d][2]benzazepine-3-carboxaldehyde in 100 ml of acetone. After 2.5 hr the mixture was diluted with a saturated aqueous solution of sodium bisulfite, neutralized with the addition of acetic acid and extracted with methylene chloride. The methylene chloride solution was dried over anhydrous sodium sulfate and concentrated at reduced pressure to dryness. Trituration of the residue with methylene chloride gave yellow crysals, mp 216°-218°. Recrystallization from a mixture of ethanol and ether gave yellow prisms, mp 252°-254° (dec).
Workup
- extractionextracted with methylene chloride
- dry with materialThe methylene chloride solution was dried over anhydrous sodium sulfate
- concentrationconcentrated at reduced pressure to dryness
- customTrituration of the residue with methylene chloride gave yellow crysals, mp 216°-218°
- customRecrystallization
- additionfrom a mixture of ethanol and ether
- customgave yellow prisms, mp 252°-254° (dec)
Sources & evidence
- ORD record
- ord-9ec19039f23e4c41a6afc0b9c92ec899
- Source dataset
- uspto-grants-1982_10
- Patent number
- US04354973
Reaction notes
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