Diethylamine → 2,8-Dimethylnona-2,7-dien-4-one

HRID 1283903Notes

Reaction equation

HRID 1283903 reaction equation
[OH-].[Na+].[O:3]=[C:4]([CH:6]=[C:7]([CH3:9])[CH3:8])[CH3:5].C(NCC)C.Cl[CH2:16][CH:17]=[C:18]([CH3:20])[CH3:19]>>[CH2:16]([CH2:5][C:4]([CH:6]=[C:7]([CH3:9])[CH3:8])=[O:3])[CH:17]=[C:18]([CH3:20])[CH3:19]

Participants

5

Conditions

Temperature
70 °C

Procedure

To a well stirred mixture of 60 g of 96% sodium hydroxide and 600 g of mesityl oxide was added 3 g of diethylamine, followed by 105 g of 94% 1-chloro-3-methyl-2-butene. The mixture was then heated to 70° C. over a 10 minute period, and the external heat source immediately removed. The mass continued to rise in temperature to 80° C. over a 10 minute period, and was then maintained at between 79° and 82° C. over a 2.3 hour period, with either heating or cooling, as needed. After cooling to 30° C., the mixture was quenched with 250 ml of water and stirred vigorously. The organic phase was then separated and the aqueous layer extracted four times with 20 ml portions of benzene. The organic phases were combined and dried overnight over sodium sulfate. The dried oil phase was then treated with 2 ml of acetic acid prior to distillation. The yield was 123.7 g of the mixture of prenyl mesityl oxide isomers.

Workup

  1. customthe external heat source immediately removed
  2. temperaturewas then maintained at between 79° and 82° C. over a 2.3 hour period
  3. temperaturewith either heating or cooling
  4. temperatureAfter cooling to 30° C.
  5. customthe mixture was quenched with 250 ml of water
  6. stirringstirred vigorously
  7. customThe organic phase was then separated
  8. extractionthe aqueous layer extracted four times with 20 ml portions of benzene
  9. dry with materialdried overnight over sodium sulfate
  10. additionThe dried oil phase was then treated with 2 ml of acetic acid
  11. distillationto distillation

Sources & evidence

ORD record
ord-1764c71d5dff4bfc9ee44d1b7ea0c3fa
Source dataset
uspto-grants-1976_08
Patent number
US03976700

Reaction notes

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