Methyl Ethyl Ketone → 2,6-Diethyl-2,3,6-trimethylpiperidin-4-one

HRID 1391227Notes

Reaction equation

HRID 1391227 reaction equation
[CH2:1]([C:3]1([CH3:14])N=[C:7]([CH2:9][CH3:10])[CH2:6][C:5]([CH2:12][CH3:13])([CH3:11])[NH:4]1)[CH3:2].C(C(C)=[O:18])C.O.O.[Cl-].[Ca+2].[Cl-].[OH-].[Na+]>O>[CH2:1]([C:3]1([CH3:14])[CH:9]([CH3:10])[C:7](=[O:18])[CH2:6][C:5]([CH2:12][CH3:13])([CH3:11])[NH:4]1)[CH3:2]

Participants

6

Conditions

Temperature
60 °C

Procedure

To an ice-cooled mixture of 39.2 g of 2,4,6-triethyl-2,6-dimethyl-1,2,5,6-tetrahydropyrimidine and 18.0 g of methyl ethyl ketone were added 14.7 g of powdered calcium chloride dihydrate, followed by 3 ml of water. The resulting mixture was heated at 60° C., with stirring, for 15 hours, made alkaline by the addition of a 35% aqueous solution of sodium hydroxide and extracted with diethyl ether. The ethereal solution was then dried over potassium carbonate and the diethyl ether was evaporated off. The residue was distilled under reduced pressure, giving 32.4 g of the title compound. Boiling point 91°-93° C./2.0 mmHg.

Workup

  1. extractionextracted with diethyl ether
  2. dry with materialThe ethereal solution was then dried over potassium carbonate
  3. customthe diethyl ether was evaporated off
  4. distillationThe residue was distilled under reduced pressure

Sources & evidence

ORD record
ord-80615356419e4ebb8cf80f3bd970e6e5
Source dataset
uspto-grants-1979_02
Patent number
US04141883

Reaction notes

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