1-Bromo-2-methylpropane → 2-(Benzylmethylamino)-3,7,11-trimethyl-3,7-dodecanediol

HRID 1708957Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1708957
C([Mg]Br)C(C)C.[Mg].C(Br)C(C)C.[CH3:13][C:14]([OH:24])([CH2:18][CH2:19][CH2:20][CH:21]([CH3:23])[CH3:22])[CH2:15][CH:16]=[CH2:17].[CH2:25]([CH2:32][NH:33][CH:34]([CH3:38])[C:35](=[O:37])[CH3:36])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.[Cl-].[NH4+]>C(OCC)C.[Cl-].[Cl-].[CH-]1C=CC=C1.[CH-]1C=CC=C1.[Ti+2]>[CH2:25]([CH2:32][NH:33][CH:34]([C:35]([CH3:36])([OH:37])[CH2:17][CH2:16][CH2:15][C:14]([CH3:13])([OH:24])[CH2:18][CH2:19][CH2:20][CH:21]([CH3:22])[CH3:23])[CH3:38])[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1

Komponenten

9

Edukt 6

HCID 65551-Bromo-2-methylpropaneHCID 25517Ammonium ChlorideHCID 5462224MagnesiumHCID 199287334,8-Dimethyl-1-nonen-4-olHCID 217862353-(Phenethylamino)-butan-2-oneHCID 178418816HCID 178418816, Verbindung

Produkt 1

HCID 199287442-(Benzylmethylamino)-3,7,11-trimethyl-3,7-dodecanediolAusbeute 17 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 124040768Titanocene dichiorideKatalysatorHCID 3283Diethyl EtherLösungsmittel2×

Versuchsvorschrift

To a solution of isobutylmagnesium bromide prepared from 14.6 g of magnesium, 68.5 g of isobutyl bromide and 500 ml of diethyl ether was added a solution of 34 g of 4,8-dimethyl-1-nonen-4-ol in 100 ml of diethyl ether dropwise under ice-cooling. After completion of the addition, 2.5 g of titanocene dichloride was added to the above solution at room temperature and the mixture was stirred at that temperature for 18 hours. Then, 38.2 g of 3-(benzylmethylamino)-2-butanone was added dropwise under ice-cooling and the mixture was stirred at that temperature for 30 minutes. The reaction mixture was poured into a saturated aqueous solution of ammonium chloride and extracted with diethyl ether. The ether was distilled off, and after addition of chloroform, the residue was washed with a saturated aqueous solution of sodium chloride and a small amount of aqueous sodium hydrogen carbonate. After drying over anhydrous sodium sulfate, the chloroform was distilled off and the residue was subjected to silica gel column chromatography (elution with 95% methylene chloride-5% triethylamine) to give 11.3 g of 2-(benzylmethyl- amino)-3,7,11-trimethyl-3,7-dodecanediol [Compound (71)]. Yield 17%.

Aufarbeitung

  1. temperaturecooling
  2. additionwas added to the above solution at room temperature
  3. temperaturecooling
  4. stirringthe mixture was stirred at that temperature for 30 minutes
  5. extractionextracted with diethyl ether
  6. distillationThe ether was distilled off
  7. additionafter addition of chloroform
  8. washthe residue was washed with a saturated aqueous solution of sodium chloride
  9. dry with materialAfter drying over anhydrous sodium sulfate
  10. distillationthe chloroform was distilled off
  11. washthe residue was subjected to silica gel column chromatography (elution with 95% methylene chloride-5% triethylamine)

Quellen und Nachweise

ORD-Eintrag
ord-66372e67de4849f8b999a37cb4631dcf
Quelldatensatz
uspto-grants-1990_08
Patentnummer
US04946857

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