3-[4-(Propan-2-yl)cyclohexyl]propanoic acid → 1,5-Bis[4-(propan-2-yl)cyclohexyl]pentan-3-one

HRID 2071875Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2071875
[CH:1]([CH:4]1[CH2:9][CH2:8][CH:7]([CH2:10][CH2:11][C:12]([OH:14])=O)[CH2:6][CH2:5]1)([CH3:3])[CH3:2]>[Fe]>[CH:1]([CH:4]1[CH2:5][CH2:6][CH:7]([CH2:10][CH2:11][C:12](=[O:14])[CH2:11][CH2:10][CH:7]2[CH2:6][CH2:5][CH:4]([CH:1]([CH3:2])[CH3:3])[CH2:9][CH2:8]2)[CH2:8][CH2:9]1)([CH3:3])[CH3:2]

Komponenten

3

Edukt 1

HCID 213966513-[4-(Propan-2-yl)cyclohexyl]propanoic acid

Produkt 1

HCID 213966471,5-Bis[4-(propan-2-yl)cyclohexyl]pentan-3-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 23925IronKatalysator

Reaktionsbedingungen

Temperatur
290 °C

Versuchsvorschrift

3-(4-Isopropylcyclohexyl)propionic acid (39.7 g., 0.20 mole) and iron (hydrogen reduced, 6.15 g., 0.11 mole) is heated for 1.5 hours at 195° C. under a nitrogen atmosphere. After that time, the temperature is increased to 290° C. and maintained at that temperature for three hours. The cooled reaction mass is extracted well with ether, filtered through Celite, and the ethereal extracts concentrated under vacuum. The residue is stripped under vacuum to leave the product, 17.3 g. (51%).

Aufarbeitung

  1. temperaturemaintained at that temperature for three hours
  2. customThe cooled reaction mass
  3. extractionis extracted well with ether
  4. filtrationfiltered through Celite
  5. concentrationthe ethereal extracts concentrated under vacuum
  6. customto leave the product, 17.3 g

Quellen und Nachweise

ORD-Eintrag
ord-b0f943ad6dc84a02889d4cc46b1df853
Quelldatensatz
uspto-grants-1977_09
Patentnummer
US04049417

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