Water → 9-(2,6,6-Trimethylcyclohex-1-en-1-yl)nonanoic acid

HRID 1055184Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1055184
[CH3:1][C:2]1[CH2:7][CH2:6][CH2:5][C:4]([CH3:9])([CH3:8])[C:3]=1[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([O:20]CC)=[O:19].[OH-].[K+].O>C(O)C>[CH3:1][C:2]1[CH2:7][CH2:6][CH2:5][C:4]([CH3:8])([CH3:9])[C:3]=1[CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([OH:20])=[O:19]

Komponenten

5

Versuchsvorschrift

To ethyl 9-(2,6,6-trimethylcyclohex-1-en-1-yl)nonanoate (13.2 g, 42.9 mmol) in ethanol (80 mL) was added 4 M KOH (43 mL). The mixture was stirred at room temperature for 1.5 h. Water (350 mL) was added and the solution was washed with tert-butyl methyl ether (2×100 mL). The SimVA, aqueous phase was cooled, acidified with 4 M HCl (˜45 mL) and extracted with pentane (3×100 mL). The combined pentane extracts were washed with water (200 mL), dried (MgSO4), filtered, concentrated and dried under high vacuum. The material was redissolved in pentane (100 mL), concentrated and dried under high vacuum one more time to give 9-(2,6,6-trimethylcyclohex-1-en-1-yl)nonanoic acid as a colorless oil (11.1 g, 92% yield). MS ESI− m/z 279 [M−H]−.

Aufarbeitung

  1. washthe solution was washed with tert-butyl methyl ether (2×100 mL)
  2. temperatureThe SimVA, aqueous phase was cooled
  3. extractionextracted with pentane (3×100 mL)
  4. washThe combined pentane extracts were washed with water (200 mL)
  5. dry with materialdried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customdried under high vacuum
  9. dissolutionThe material was redissolved in pentane (100 mL)
  10. concentrationconcentrated
  11. customdried under high vacuum one more time

Quellen und Nachweise

ORD-Eintrag
ord-5fe86ae9af884f709a9b3c85a2e5e7fa
Quelldatensatz
uspto-grants-2016_07
Patentnummer
US09393315B2

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