Hydrochloric Acid → HCID 19823812, compound

HRID 1650945Notes

Reaction equation

HRID 1650945 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]=1

Participants

7

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

  1. extractionThe resulting mixture was extracted with ether
  2. washthe ether extracts were washed with water
  3. customdried
  4. customRemoval of the solvent
  5. customgave an oil which
  6. customThe residue after the removal of the solvents
  7. 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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