Hydrochloric Acid → HCID 19823812, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([CH:12]([N:16]([CH3:18])[CH3:17])[C:13](=[O:15])[CH3:14])[CH2:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[BH4-].[Na+].S(=O)(=O)(O)O.Cl>C(O)C.CC(O)C>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2([CH:12]([N:16]([CH3:17])[CH3:18])[CH:13]([OH:15])[CH3:14])[CH2:9][CH2:10][CH2:11]2)=[CH:6][CH:7]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 1-[1-(4-chlorophenyl)cyclobutyl]-1-dimethylaminopropan-2-one (1.9 g prepared as described in Example 47) in ethanol (10 ml) was added dropwise to a suspension of sodium borohydride (0.4 g) in ethanol (20 ml) and the mixture was stirred for 4 hours at ambient temperature. 5N Sulphuric acid (10 ml) was added and then the acidified mixture was basified. The resulting mixture was extracted with ether and the ether extracts were washed with water and dried. Removal of the solvent gave an oil which was converted into a hydrochloride salt by treatment with a mixture of excess concentrated hydrochloric acid and propan-2-ol. The residue after the removal of the solvents were dried by azeotropic distillation with propan-2-ol to give 1-[1-(4-chlorophenyl)cyclobutyl]-1-dimethylaminopropan-2-ol hydrochloride (m.p. 255° C.).
Workup
- extractionThe resulting mixture was extracted with ether
- washthe ether extracts were washed with water
- customdried
- customRemoval of the solvent
- customgave an oil which
- customThe residue after the removal of the solvents
- dry with materialwere dried by azeotropic distillation with propan-2-ol
Sources & evidence
- ORD record
- ord-a69d6f96cc2d4cef8ba99e35f886cb2d
- Source dataset
- uspto-grants-1990_05
- Patent number
- US04925879
Reaction notes
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