Methanol → HCID 17821171, Verbindung

HRID 1169169

Reaktionsgleichung

Reaktionsgleichung von HRID 1169169
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:19]=[CH:18][CH:17]=[C:16]3[C:12]=2[CH2:13][CH2:14][C:15]3=O)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[BH4-].[Na+].CO.[Cl-].[NH4+]>C1(C)C=CC=CC=1>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([C:11]2[CH:19]=[CH:18][CH:17]=[C:16]3[C:12]=2[CH:13]=[CH:14][CH2:15]3)=[CH:7][CH:6]=1)([CH3:4])([CH3:2])[CH3:3]

Komponenten

6

Edukt 4

HCID 887MethanolHCID 25517Ammonium ChlorideHCID 4311764Sodium borohydrideHCID 229905194-(4-tert-Butyl-phenyl)-indan-1-one

Produkt 1

HCID 17821171HCID 17821171, VerbindungAusbeute 86,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

9.0 g (34 mmol) of 4-(4′-tert-butylphenyl)indanone and 1.3 g (34 mmol) of sodium borohydride together with 32 ml of toluene are placed in a reaction vessel. The reaction mixture is heated to 50° C., after which 6.2 ml (148 mmol) of methanol are added over a period of 10 minutes. After the addition is complete, the mixture is stirred at 50° C. for 2 hours. After addition of 30 ml of a saturated ammonium chloride solution, the mixture is stirred for another 30 minutes. After separating off the aqueous phase, the organic phase is washed once with a saturated ammonium chloride solution and once with a saturated sodium chloride solution. After drying over magnesium sulfate, the solvent mixture is removed on a rotary evaporator, the residue is made up to a total volume of 150 ml with toluene and is admixed with 0.2 g of p-toluenesulfonic acid. After 30 minutes, no more elimination of water is observed. The reaction mixture is subsequently washed once with a saturated sodium hydrogen carbonate solution, then dried over magnesium sulfate and the solvent is removed in an oil pump vacuum. 7.3 g (86%) of the desired product are isolated.

Aufarbeitung

  1. additionAfter the addition
  2. stirringthe mixture is stirred for another 30 minutes
  3. customAfter separating off the aqueous phase
  4. washthe organic phase is washed once with a saturated ammonium chloride solution and once with a saturated sodium chloride solution
  5. dry with materialAfter drying over magnesium sulfate
  6. customthe solvent mixture is removed on a rotary evaporator
  7. waitAfter 30 minutes
  8. washThe reaction mixture is subsequently washed once with a saturated sodium hydrogen carbonate solution
  9. dry with materialdried over magnesium sulfate
  10. customthe solvent is removed in an oil pump vacuum

Quellen und Nachweise

ORD-Eintrag
ord-ce94f439f2de4510ac7e59c2d5984922
Quelldatensatz
uspto-grants-2003_09
Patentnummer
US06627764B1

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