Reacción #75275

ord-5abf4bc882194c00b49013a92b58a98e

Ecuación de reacción

CC(=O)C1CCCC(C)(C)C1
1-acetyl-3,3-dimethylcyclohexane
[Na+].[OH-]
sodium hydroxide
C=C(C)CCl
methallyl chloride
Cc1ccccc1
toluene
CC(=O)C1CCCC(C)(C)C1
1-acetyl-3,3,-dimethylcyclohexane
C=C(C)CC1(C(C)=O)CCCC(C)(C)C1
1-acetyl-3,3-dimethyl-1-methallyl cyclohexane

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturaat reflux for 4 1/4 hours
  2. 2
    workup.DISTILLATIONthe organic layer is distilled rapidly through a short column

Procedimiento

A slurry of 1-acetyl-3,3-dimethylcyclohexane (624 grams, 4 moles), granular sodium hydroxide (240 grams, 6 moles), Aliquot® 336 (tricaprylmethylammonium chloride [35 grams]), methallyl chloride (432 grams, 4.8 moles), and 400 ml of toluene is heated at reflux for 4 1/4 hours. At the end of this time, one liter of water is added to the cooled reaction mass. The aqueous layer is discarded, and the organic layer is distilled rapidly through a short column to afford 203 grams of recovered 1-acetyl-3,3,-dimethylcyclohexane, 500 grams of 1-acetyl-3,3-dimethyl-1-methallyl cyclohexane, and 73 grams of 3,3-dimethyl-1-(2-methyllyl-5-methyl-4-pentenoyl)cyclohexane) (1°-4°, 3.0 mm Hg) containing 5% of 3,3-dimethyl-1-(4-methyl-4-pentenoyl). A portion of the latter compound is isolated by GLC chromatography (1'×1/4" 80% SE-30 packed column; 200° C. isothermal) and exhibits the following odor and flavor properties:

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04175569uspto-grants-1979_11