Hydrochloric Acid → HCID 21519265, compound
Reaction equation
Cl.[CH3:2][CH:3]([C:11]1([OH:23])[CH2:16][CH2:15][CH2:14][CH2:13][CH:12]1[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)[CH2:4][N:5]1[CH2:10][CH2:9][O:8][CH2:7][CH2:6]1.[C:24]([Cl:27])(=[O:26])[CH3:25].[OH-].[Na+].Cl>CCOCC>[ClH:27].[C:24]([O:23][C:11]1([CH:3]([CH3:2])[CH2:4][N:5]2[CH2:10][CH2:9][O:8][CH2:7][CH2:6]2)[CH2:16][CH2:15][CH2:14][CH2:13][CH:12]1[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)(=[O:26])[CH3:25]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
1-(1-Methyl-2-morpholinoethyl)-2-phenylcyclohexanol hydrochloride (Example XVIII) is converted to the free base and treated with acetyl chloride according to the procedure of Example I (c) using 14 ml acetyl chloride and a reaction time of 90 hours. The product is treated with NaOH to give the base which is dissolved in ether and acidified with HCl gas to give 10.7 g., m. 176.5-7.5 after recrystallization from isopropanol.
Workup
- customa reaction time of 90 hours
- customto give the base which
- customto give 10.7 g
- custom176.5-7.5 after recrystallization from isopropanol
Sources & evidence
- ORD record
- ord-34cb46103967494191ad32c2aca5a87b
- Source dataset
- uspto-grants-1976_08
- Patent number
- US03974157
Reaction notes
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