Diethyl Ether → Benzeneacetic acid, 4-ethoxy-alpha-methylene-, ethyl ester

HRID 1105503

Reaktionsgleichung

Reaktionsgleichung von HRID 1105503
C([C:3]1[C:4](CC)=[C:5]([CH:12]([C:16](C(O)=O)=O)[C:13]([O-:15])=[O:14])[CH:6]=[CH:7][C:8]=1[O:9][CH2:10][CH3:11])C.C(=O)([O-])[O-].[K+].[K+].[CH3:29][CH2:30]OCC>C=O>[CH2:29]([O:15][C:13](=[O:14])[C:12]([C:5]1[CH:4]=[CH:3][C:8]([O:9][CH2:10][CH3:11])=[CH:7][CH:6]=1)=[CH2:16])[CH3:30]

Komponenten

5

Edukt 3

HCID 3283Diethyl EtherHCID 11430Potassium CarbonateHCID 131711858Diethyl-2-p-ethoxyphenyl-oxaloacetate

Produkt 1

HCID 6454764Benzeneacetic acid, 4-ethoxy-alpha-methylene-, ethyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 712FormaldehydeLösungsmittel

Versuchsvorschrift

The keto-ester III (143.8 g) was stirred in dilute formaldehyde solution (62 ml 37% formaldehyde+water 220 ml) and to the suspension potassium carbonate solution (54.5 g, in water 280 ml) was added dropwise. At the end of the addition, ether was added to the stirred suspension to dissolve the gummy precipitate which formed and after an additional 15 minutes, gas evolution commenced. When this gas evolution ceased (after about 2 hours) the reaction mixture was extracted with additional ether and the combined ether extracts were washed with water and evaporated after drying with Na2SO4. The yield of the ethyl-2-(p-ethoxyphenyl)acrylate (II) (isolated as a yellow oil) was 97.8 g (79.8%).

Aufarbeitung

  1. additionwas added dropwise
  2. additionwas added to the stirred suspension
  3. dissolutionto dissolve the gummy precipitate which
  4. customformed and after an additional 15 minutes
  5. custom(after about 2 hours)
  6. extractionwas extracted with additional ether
  7. washthe combined ether extracts were washed with water
  8. customevaporated
  9. dry with materialafter drying with Na2SO4

Quellen und Nachweise

ORD-Eintrag
ord-35a12217359e4f7db8f3147f4205cffc
Quelldatensatz
uspto-grants-1982_01
Patentnummer
US04309350

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