Hydroxyamine hydrochloride → 1-benzyl-4-chloro-5-hydroxyiminomethyl-2,3,6,7-tetrahydro-1H-azepine
Reaction equation
Cl.[CH2:2]([N:9]1[CH2:15][CH2:14][C:13]([CH:16]=O)=[C:12]([Cl:18])[CH2:11][CH2:10]1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Cl.[NH2:20][OH:21]>C(O)C>[CH2:2]([N:9]1[CH2:15][CH2:14][C:13]([CH:16]=[N:20][OH:21])=[C:12]([Cl:18])[CH2:11][CH2:10]1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1Participants
4
Procedure
Prepared by reacting 1-benzyl-4-chloro-5-formyl-2,3,6,7-tetrahydro-1H-azepine hydrochloride with hydroxylamine hydrochloride in ethanol at 30° C.
Workup
- customPrepared
- customat 30° C.
Sources & evidence
- ORD record
- ord-ab994e9d2b3e4cf0ba7ff85502ef1a00
- Source dataset
- uspto-grants-1998_10
- Patent number
- US05827849
Reaction notes
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