Hydrochloric Acid → 4-(Dimethylamino)cyclohexan-1-one

HRID 1387971Notes

Reaction equation

HRID 1387971 reaction equation
C1O[C:4]2([CH2:9][CH2:8][C:7](=O)[CH2:6][CH2:5]2)[O:3]C1.Cl.[CH3:13][NH:14][CH3:15].C(N(CC)CC)C.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.Cl>ClCCCl.O>[CH3:13][N:14]([CH3:15])[CH:7]1[CH2:8][CH2:9][C:4](=[O:3])[CH2:5][CH2:6]1

Participants

8

Procedure

To a suspension of 1,4-cyclohexanedione monoethyleneketal (3.82 g, 24.6 mmol) and dimethylamine hydrochloride (2.00 g, 24.6 mmol) in 1,2-dichloroethane (50 ml) were dropwise added triethylamine (4.2 ml, 29.6 mmol) and DBU (1,8-diazabicyclo-[5.4.0]-7-undecene) (4.4 ml), and the mixture was stirred for 10 minutes. To the mixture was added triacetoxyborohydride (7.68 g, 34.4 mmol), and the mixture was stirred for 4.5 hours. Precipitate was filtered off, and the filtrate was concentrated to give crude product (6.34 g), which was dissolved in water (10 ml). To the mixture was dropwise added concentrated hydro-chloric acid (6 ml), and the mixture was stirred for 48 hours. The reaction mixture was diluted with water and washed twice with ether. The aqueous layer was made basic with sodium hydroxide and extracted with ether twice. The extract was washed with saturated sodium chloride solution, dried with potassium carbonate and purified by evaporation to give 4-dimethylaminocyclohexanone (0.59 g, 17%).

Workup

  1. stirringthe mixture was stirred for 4.5 hours
  2. filtrationPrecipitate was filtered off
  3. concentrationthe filtrate was concentrated
  4. customto give crude product (6.34 g), which
  5. stirringthe mixture was stirred for 48 hours
  6. washwashed twice with ether
  7. extractionextracted with ether twice
  8. washThe extract was washed with saturated sodium chloride solution
  9. dry with materialdried with potassium carbonate
  10. custompurified by evaporation

Sources & evidence

ORD record
ord-dead5506803344a391c54695092a67c7
Source dataset
uspto-grants-2001_07
Patent number
US06268354B1

Reaction notes

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