Sodium hydride → Ethyl 5-methyl-2-heptenoate

HRID 1167895Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1167895
[H-].[Na+].C[CH:4]([CH2:8][CH3:9])[CH2:5][CH:6]=[O:7]>CCCCCC.C(COC)OC.COCC>[CH3:4][CH:9]([CH2:5][CH3:6])[CH2:8][CH:4]=[CH:5][C:6]([O:7][CH2:9][CH3:8])=[O:7]

Komponenten

6

Edukt 2

HCID 24758Sodium hydrideHCID 275233-Methylvaleraldehyde

Produkt 1

HCID 53937332Ethyl 5-methyl-2-heptenoateAusbeute 122 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 8058HexaneLösungsmittelHCID 80711,2-DimethoxyethaneLösungsmittelHCID 10903MethoxyethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

Sodium hydride (60% dispersion, 2.4 g, 65 mmol) was washed with hexane and suspended in dimethoxyethane 60 mL. While cooling in ice water bath triethyl phosphonoacetate was slowly added, calcd. 5 minutes. The reaction was stirred for 15 minutes at 0° C. and a solution of 3-methyl-1-pentanal 11 (6.5 g, 65 mmol) in methoxyethane 20 mL was added. After refluxing overnight, it was concentrated, water and hexane were added, the organic phase was separated, and the aqueous portion discarded. The solution was washed twice with brine and dried on magnesium sulfate. The solvent was evaporated to give 12 (6.75 g, 61%).

Aufarbeitung

  1. additionwas slowly added
  2. custom5 minutes
  3. temperatureAfter refluxing overnight
  4. concentrationit was concentrated
  5. additionwater and hexane were added
  6. customthe organic phase was separated
  7. washThe solution was washed twice with brine
  8. customdried on magnesium sulfate
  9. customThe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-fa44334c62744af09529b17dad9131fd
Quelldatensatz
uspto-grants-2003_09
Patentnummer
US06620829B2

Notizen zur Reaktion

Wird geladen…