Hydrochloric Acid → HCID 19823639, compound

HRID 1650949Notes

Reaction equation

HRID 1650949 reaction equation
[CH3:1][N:2]([CH3:20])[CH:3]([C:9]1([C:13]2[CH:18]=[CH:17][C:16]([CH3:19])=[CH:15][CH:14]=2)[CH2:12][CH2:11][CH2:10]1)[C:4](=[O:8])[CH2:5][CH2:6][CH3:7].O.Cl>O1CCCC1>[CH3:20][N:2]([CH3:1])[CH:3]([C:9]1([C:13]2[CH:18]=[CH:17][C:16]([CH3:19])=[CH:15][CH:14]=2)[CH2:12][CH2:11][CH2:10]1)[CH:4]([OH:8])[CH2:5][CH2:6][CH3:7]

Participants

5

Procedure

Boranedimethylsulphide complex (3 ml) was added dropwise under nitrogen over a period of 20 minutes to a solution of 1-dimethylamino-1-[1-(4-tolyl)cyclobutyl]pentan-2-one (1.85 g preprared as described in Example 16) in tetrahydrofuran (20 ml) and the resulting mixture stirred for 3 days at ambient temperature. The mixture was cooled to 0° C. and water (25 ml) and then 5N hydrochloric acid (25 ml) added. The mixture was basified and the tetrahydrofuran removed by evaporation. The residue was extracted with ether and the extracts washed with water, dried, filtered and evaporated to give an oil which was dissolved in petroleum ether (b.p. 80°-100° C.) and purified on a column packed with magnesia-silica gel sold under the trade name Florisil using petroleum ether (b.p. 80° to 100° C.) as eluant. The eluate was evaporated to give an oil which was distilled (215° C./1.5 mm Hg) to give 1-dimethylamino-1-[ 1-(4-tolyl)cyclobutyl]pentan-2-ol.

Workup

  1. temperatureThe mixture was cooled to 0° C.
  2. customthe tetrahydrofuran removed by evaporation
  3. extractionThe residue was extracted with ether
  4. washthe extracts washed with water
  5. customdried
  6. filtrationfiltered
  7. customevaporated
  8. customto give an oil which
  9. custompurified on a column
  10. customThe eluate was evaporated
  11. customto give an oil which
  12. distillationwas distilled (215° C./1.5 mm Hg)

Sources & evidence

ORD record
ord-fe0c3ddfb5da4f40814222a6c5baba4a
Source dataset
uspto-grants-1990_05
Patent number
US04925879

Reaction notes

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