Water → 3-(Dimethoxymethyl)-4,4-dimethoxybutanenitrile

HRID 524856Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 524856
[CH3:1][O:2][CH:3]([O:16][CH3:17])[CH:4]([CH:11]([O:14][CH3:15])[O:12][CH3:13])[CH2:5][CH2:6]S([O-])(=O)=O.C(OCC)(=O)C.O.CC#[N:27]>[C-]#N.C([N+](CC)(CC)CC)C>[CH3:1][O:2][CH:3]([O:16][CH3:17])[CH:4]([CH:11]([O:14][CH3:15])[O:12][CH3:13])[CH2:5][C:6]#[N:27]

Komponenten

6

Edukt 4

HCID 962WaterHCID 6342AcetonitrileHCID 8857Ethyl AcetateHCID 86720913[2-(Dimethoxymethyl)-3,3-dimethoxypropyl]methanesulfonate

Produkt 1

HCID 867208913-(Dimethoxymethyl)-4,4-dimethoxybutanenitrile

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3014735Tetraethylammonium cyanideKatalysator

Versuchsvorschrift

Tetraethylammonium cyanide (142.3 g, 910.8 mmol) was added portionwise over 10 minutes to a solution of [2-(dimethoxymethyl)-3,3-dimethoxypropyl]methanesulfonate (124 g, 455.4 mmol) in MeCN (1.24 L). The reaction mixture was stirred at room temperature for 72 h, then portioned between ethyl acetate (1.24 L) and water (1.24 L). The layers were separated and the organic layer was isolated, washed with brine. The organics were dried over MgSO4, filtered and evaporated to give 3-(dimethoxymethyl)-4,4-dimethoxybutanenitrile 11 as a dark brown oil (86.1 g).

Aufarbeitung

  1. customThe layers were separated
  2. customthe organic layer was isolated
  3. washwashed with brine
  4. dry with materialThe organics were dried over MgSO4
  5. filtrationfiltered
  6. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-38aa866f0166481b9bbb06105e9e60d1
Quelldatensatz
uspto-grants-2016_05
Patentnummer
US09340546B2

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