Ethanol → HCID 3067727, compound
Reaction equation
[ClH:1].[NH2:2][OH:3].[N:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH2:10]([OH:12])[CH3:11]>>[Cl:1][C:6]1[CH:5]=[C:8]2[C:9](=[CH:8][CH:7]=1)[N:4]([C:10](=[O:12])[CH3:11])[CH2:5][CH2:6][C:7]2=[N:2][OH:3]Participants
4
Procedure
Then, the above product was dissolved in 300 ml of ethanol, to which were added 15.64 parts of hydroxylamine hydrochloride and 17.8 parts of pyridine, and the reaction was effected under reflux for 1.5 hours. Thereafter, the product was treated as in Example 1 to obtain 20.4 parts of 6-chloro-4-oximino-1-acetyl-1,2,3,4-tetrahydroquinoline as white crystals.
Workup
- temperatureunder reflux for 1.5 hours
- additionThereafter, the product was treated as in Example 1
Sources & evidence
- ORD record
- ord-8d4220ad08504bc1ad08152e1cef24dd
- Source dataset
- uspto-grants-1983_12
- Patent number
- US04421919
Reaction notes
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