Morpholine → 4-Isopropenyl-1-methyl-2-morpholin-4-yl-cyclohexanol

HRID 1432513Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1432513
[CH3:1][C:2]([CH:4]1[CH2:9][CH:8]2[O:10][C:7]2([CH3:11])[CH2:6][CH2:5]1)=[CH2:3].[Cl-].[Li+].[NH:14]1[CH2:19][CH2:18][O:17][CH2:16][CH2:15]1>C(O)C>[C:2]([CH:4]1[CH2:5][CH2:6][C:7]([CH3:11])([OH:10])[CH:8]([N:14]2[CH2:19][CH2:18][O:17][CH2:16][CH2:15]2)[CH2:9]1)([CH3:1])=[CH2:3]

Komponenten

5

Edukt 3

HCID 8083MorpholineHCID 91496Limonene oxideHCID 433294Lithium Chloride

Produkt 1

HCID 226252054-Isopropenyl-1-methyl-2-morpholin-4-yl-cyclohexanolAusbeute 49,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

(+)-Limonene oxide (13.2 g, 0.087 moles) was dissolved in ethanol (40 ml) and lithium chloride (5.9 g, 0.14 moles) was added with stirring. Morpholine (11.4 g, 0.13 moles) was added and the reaction mixture was heated at 60° for 48 hours. The solvent was evaporated under reduced pressure and the residue taken up in dichloromethane. Washed with water. Extracted into 2M hydrochloric acid and washed with dichloromethane. Basified to pH 10 by addition of 2M sodium hydroxide. Extracted with diethyl ether and washed with water. Dried over anhydrous magnesium sulphate and evaporated the solvent under reduced pressure to give the product as a yellow oil (10.3 g)

Aufarbeitung

  1. temperaturethe reaction mixture was heated at 60° for 48 hours
  2. customThe solvent was evaporated under reduced pressure
  3. washWashed with water
  4. extractionExtracted into 2M hydrochloric acid
  5. washwashed with dichloromethane
  6. additionBasified to pH 10 by addition of 2M sodium hydroxide
  7. extractionExtracted with diethyl ether
  8. washwashed with water
  9. dry with materialDried over anhydrous magnesium sulphate
  10. customevaporated the solvent under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-c0101af3432a49f284274d69e85e6902
Quelldatensatz
uspto-grants-2009_11
Patentnummer
US07612101B2

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