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Water → 3-[p-(3-Hydroxy-2-methyl-1-propenyl)benzyl]pyridine

HRID 986463
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 986463
Cl[CH:2]([C:7]1[CH:19]=[CH:18][C:10]([CH2:11][C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)=[CH:9][CH:8]=1)[CH:3]([CH3:6])[CH2:4][OH:5].C1CCN2C(=NCCC2)CC1.O>CN(C)C=O>[OH:5][CH2:4][C:3]([CH3:6])=[CH:2][C:7]1[CH:19]=[CH:18][C:10]([CH2:11][C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)=[CH:9][CH:8]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 137455293-[p-(1-Chloro-3-hydroxy-2-methylpropyl)benzyl]pyridine

Produkt 1

HCID 543469663-[p-(3-Hydroxy-2-methyl-1-propenyl)benzyl]pyridineAusbeute 62,7 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

In 1.3 ml of N,N-dimethylformamide was dissolved 260 mg of 3-[p-(1-chloro-3-hydroxy-2-methylpropyl)benzyl]pyridine, and 0.28 ml of DBU was added to the resulting solution after which the resulting mixture was subjected to reaction at a temperature of 110° to 120° C. for one hour. To the reaction mixture was added 5 ml of water, and the mixture was subjected to extraction with two 5-ml portions of ethyl acetate. The extracts were combined, washed with 3 ml of water, and then dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and the residue thus obtained was purified by a colomn chromatography [Wako Silica Gel C-200, eluant: benzene:ethyl acetate (3:1 by volume)] to obtain 150 mg (yield 62.7%) of colorless, oily 3-[p-(3-hydroxy-2-methyl-1-propenyl)benzyl]pyridine.

Aufarbeitung

  1. additionwas added to the resulting solution after which the resulting mixture
  2. customwas subjected to reaction at a temperature of 110° to 120° C. for one hour
  3. extractionthe mixture was subjected to extraction with two 5-ml portions of ethyl acetate
  4. washwashed with 3 ml of water
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customThe solvent was removed by distillation under reduced pressure
  7. customthe residue thus obtained
  8. customwas purified by a colomn chromatography [Wako Silica Gel C-200, eluant: benzene:ethyl acetate (3:1 by volume)]

Quellen und Nachweise

ORD-Eintrag
ord-fb42811e02134d98a1d7ce7aeddff033
Quelldatensatz
uspto-grants-1987_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04713387

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