Réaction #1702071

ord-a8ca9bdf5ab14709826d641b7c67819d

Équation de réaction

Cc1ccc2c(c1)C(C)(C)CCC2(C)C
5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-methylnaphthalene
[K+].[O]=[Mn](=[O])(=[O])[O-]
potassium permanganate
[Na+].[OH-]
sodium hydroxide
[K+].[O]=[Mn](=[O])(=[O])[O-]
KMnO4
[K+].[O]=[Mn](=[O])(=[O])[O-]
potassium permanganate
CC1(C)CCC(C)(C)c2cc(C(=O)O)ccc21
5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenecarboxylic acid

Solvants

Conditions de réaction

Température
95°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    FiltrationThe reaction solution was filtrated by celite
  2. 2
    workup.ADDITIONby adding hydrochloric acid
  3. 3
    ExtractionAfter extraction by ethyl acetate
  4. 4
    Séchagethe liquid was dried over magnesium sulfate
  5. 5
    Concentrationconcentrated under reduced pressure
  6. 6
    AutreThe crude product was purified by silica gel chromatography

Mode opératoire

The synthesis process is as set forth in the chemical reaction formula below. The KMnO4 in the reaction path stands for potassium permanganate. To 5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-methylnaphthalene (3.52 g, 17.4 mmol) were added pyridine (12 mL), potassium permanganate (6.70 g, 42.4 mmol), and sodium hydroxide (1.00 g, 25.0 mmol) followed by stirring at 95° C. for 5 hours. The reaction solution was filtrated by celite and the filtrate was made acidic by adding hydrochloric acid. After extraction by ethyl acetate, the liquid was dried over magnesium sulfate, and concentrated under reduced pressure. The crude product was purified by silica gel chromatography using hexane/ethyl acetate (4/1) as an elution solvent. The yield was 141.6 mg (3%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08765719B2uspto-grants-2014_07