1-Butanol → HCID 14422895, compound
Reaction equation
[Cl:1][CH2:2][CH2:3][CH:4]([OH:16])[CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([N+:13]([O-:15])=[O:14])=[CH:9][CH:8]=1.[C:17]1([N:23]2[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]2)[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.C(=O)([O-])[O-].[Na+].[Na+].C(O)CCC>Cl>[ClH:1].[ClH:1].[N+:13]([C:10]1[CH:11]=[CH:12][C:7]([O:6][CH2:5][CH:4]([OH:16])[CH2:3][CH2:2][N:26]2[CH2:27][CH2:28][N:23]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH2:24][CH2:25]2)=[CH:8][CH:9]=1)([O-:15])=[O:14]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
This compound was prepared according to the procedure of Example 25. A mixture of 12.3 g (0.05 mole) of 4-chloro-1-(4-nitrophenoxy)-2-butanol, 8.1 g (0.05 mole) of 1-phenylpiperazine, and 26.0 g (0.25 mole) of anhydrous sodium carbonate in a total volume of 250 ml of 1-butanol gave a golden oil as residue. The hydrochloride was formed in ethereal hydrogen chloride and the collected solid was recrystallized thrice from methanol-water to give 1.1 g (5%) of white solid, m.p. 195°-200° C.
Workup
- customThis compound was prepared
- customgave a golden oil as residue
Sources & evidence
- ORD record
- ord-48ad545c80d64ae0b07b5b7f028ce923
- Source dataset
- uspto-grants-1989_11
- Patent number
- US04882330
Reaction notes
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