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Dimethylformamide → 4-Bromo-3-(hydroxymethyl)benzonitrile

HRID 1664297
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1664297
[Br:1][C:2]1[CH:9]=[CH:8][C:7](O[Si](C(C)(C)C)(C)C)=[CH:6][C:3]=1[CH2:4][OH:5].[Cl-].COC[P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.CC(C)([O-])C.[K+].[CH3:47][N:48](C)C=O>>[Br:1][C:2]1[CH:9]=[CH:8][C:7]([C:47]#[N:48])=[CH:6][C:3]=1[CH2:4][OH:5]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 6228DimethylformamideHCID 2723798Methoxymethyl-triphenylphosphonium chlorideHCID 23665647Potassium tert-butoxideHCID 67310582HCID 67310582, Verbindung

Produkt 1

HCID 534078974-Bromo-3-(hydroxymethyl)benzonitrile

Versuchsvorschrift

A mixture of 2 (20.0 mmol), (methoxymethyl)triphenylphosphonium chloride (8.49 g, 24.0 mmol), and potassium tert-butoxide (2.83 g, 24.0 mol) in N,N-dimethylformamide (50 mL) was stirred at room temperature for overnight. The reaction was quenched with 6 N HCl, and the mixture was extracted with ethyl acetate. The organic layer was washed with water (×2) and brine, and dried on anhydrous sodium sulfate. The solvent was removed under reduced. To the residue were added tetrahydrofuran (60 mL) and 6 N HCl, and the mixture was heated at reflux for 8 h. Water was added, and the mixture was extracted with ether. The organic layer was washed with brine and dried on anhydrous sodium sulfate. The solvent was removed under reduced pressure to afford 16.6 mmol of 9.

Aufarbeitung

  1. customThe reaction was quenched with 6 N HCl
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with water (×2) and brine
  4. dry with materialdried on anhydrous sodium sulfate
  5. customThe solvent was removed
  6. additionTo the residue were added tetrahydrofuran (60 mL) and 6 N HCl
  7. temperaturethe mixture was heated
  8. temperatureat reflux for 8 h
  9. additionWater was added
  10. extractionthe mixture was extracted with ether
  11. washThe organic layer was washed with brine
  12. dry with materialdried on anhydrous sodium sulfate
  13. customThe solvent was removed under reduced pressure

Quellen und Nachweise

ORD-Eintrag
ord-c603e60534e44b48a386a5796672f399
Quelldatensatz
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08039451B2

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