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Benzaldehyde → 2-(Dimethoxymethyl)-3-phenylacrylonitrile

HRID 496819
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 496819
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:9][O:10][CH:11]([O:15][CH3:16])[CH2:12][C:13]#[N:14].C[O-].[Na+]>CO>[CH3:9][O:10][CH:11]([O:15][CH3:16])[C:12](=[CH:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)[C:13]#[N:14]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 240BenzaldehydeHCID 937313,3-DimethoxypropiononitrileHCID 10942334Sodium Methoxide

Produkt 1

HCID 538099012-(Dimethoxymethyl)-3-phenylacrylonitrileAusbeute 68 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

Benzaldehyde (79.5 g, 0.75 mol) and 3,3-dimethoxypropionitrile (115.1 g, 1.0 mol) were mixed together and added to a solution of sodium methoxide (54.0 g, 1.0 mol) in methanol (400 mL) over a period of 15 minutes. The mixture was stirred at room temperature overnight. Most of the methanol was evaporated in vacuo and the residue was partitioned between ethyl acetate (500 mL) and water (450 mL). The organic layer was separated, washed with brine (400 mL), dried (MgSO4) and the solvent evaporated in vacuo. The residual oil was distilled to give 103 g (68%) of the product as a colorless oil, bp 125-130° C. (2 mm Hg).

Aufarbeitung

  1. customMost of the methanol was evaporated in vacuo
  2. customthe residue was partitioned between ethyl acetate (500 mL) and water (450 mL)
  3. customThe organic layer was separated
  4. washwashed with brine (400 mL)
  5. dry with materialdried (MgSO4)
  6. customthe solvent evaporated in vacuo
  7. distillationThe residual oil was distilled

Quellen und Nachweise

ORD-Eintrag
ord-2dbbaa9df03f4353865da47aa9bc6ae9
Quelldatensatz
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06946554B2

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