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2-Butyne-1,4-diol → (4-Hydroxy-but-2-ynyloxy)-acetonitrile

HRID 349368
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 349368
[H-].[Na+].[CH2:3]([OH:8])[C:4]#[C:5][CH2:6][OH:7].Br[CH2:10][C:11]#[N:12]>C1COCC1>[OH:7][CH2:6][C:5]#[C:4][CH2:3][O:8][CH2:10][C:11]#[N:12]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 80662-Butyne-1,4-diolHCID 11534BromoacetonitrileHCID 24758Sodium hydride

Produkt 1

HCID 86012515(4-Hydroxy-but-2-ynyloxy)-acetonitrileAusbeute 29 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Sodium hydride (60% dispersion in oil, 7.5 g, 188 mmol) was added to a solution of 2-butyne-1,4-diol (16.1 g, 187 mmol) in THF (150 mL) at 0° C. under nitrogen. After 1 h at 0° C., bromoacetonitrile (8.33 mL, 120 mmol) was added slowly and the reaction was allowed to warm to rt. After 22 h at rt, the reaction was quenched with 1 N HCl (150 mL) and extracted with EtOAc (3×150 mL). The combined extracts were washed with brine (150 mL), dried (Na2SO4), filtered and concentrated in vacuo. Purification of the residue by flash column chromatography on silica gel (CH2Cl2→2% MeOH/CH2Cl2, gradient) afforded 4.35 g (29%) of (4-hydroxy-but-2-ynyloxy)-acetonitrile.

Aufarbeitung

  1. waitAfter 22 h at rt
  2. customthe reaction was quenched with 1 N HCl (150 mL)
  3. extractionextracted with EtOAc (3×150 mL)
  4. washThe combined extracts were washed with brine (150 mL)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customPurification of the residue by flash column chromatography on silica gel (CH2Cl2→2% MeOH/CH2Cl2, gradient)

Quellen und Nachweise

ORD-Eintrag
ord-a0263dc918064c5f93fc19fbc61dc920
Quelldatensatz
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07179820B2

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