Diethyl Ether → alpha-Methyl-4-(3-pyridylmethyl)benzyl alcohol

HRID 1680032Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1680032
C[Mg]I.COC(=O)/[CH:7]=[CH:8]/[C:9]1[CH:14]=[CH:13][C:12]([CH2:15][C:16]2[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=2)=[CH:11][CH:10]=1.[Cl-].[NH4+].C([O:27]CC)C>O1CCCC1>[CH3:7][CH:8]([OH:27])[C:9]1[CH:14]=[CH:13][C:12]([CH2:15][C:16]2[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=2)=[CH:11][CH:10]=1

Komponenten

6

Edukt 4

HCID 3283Diethyl EtherHCID 25517Ammonium ChlorideHCID 12882181(E)-3-[4-(3-Pyridylmethyl)phenyl]acrylic acid methyl esterHCID 178418373HCID 178418373, Verbindung

Produkt 1

HCID 12904574alpha-Methyl-4-(3-pyridylmethyl)benzyl alcohol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Under an atmosphere of nitrogen, 1.5 ml of a 3M solution of methylmagnesium iodide in diethyl ether were added to a solution of 830 mg of the aldehyde (prepared as described in Reference Example 1) in 20 ml of tetrahydrofuran at -70° C., the mixture was allowed to warm from -70° C. to room temperature over a period of one hour with stirring, poured into a saturated aqueous solution of amonium chloride, and extracted with diethyl ether. The extract was washed with water, and a saturated aqueous solution of sodium chloride, dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixture of cyclohexane and ethyl acetate (1:1) as eluent to give 547 mg of the title compound having the following physical characteristics:

Aufarbeitung

  1. temperatureto warm from -70° C. to room temperature over a period of one hour
  2. extractionextracted with diethyl ether
  3. washThe extract was washed with water
  4. dry with materiala saturated aqueous solution of sodium chloride, dried over sodium sulphate
  5. concentrationconcentrated under reduced pressure
  6. customThe residue was purified by column chromatography on silica gel using
  7. additiona mixture of cyclohexane and ethyl acetate (1:1) as eluent

Quellen und Nachweise

ORD-Eintrag
ord-9c7654cb19684b5da6fd89394368c8b3
Quelldatensatz
uspto-grants-1981_06
Patentnummer
US04271170

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