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Pyridine → Ethyl 4-(methoxycarbonylmethoxy)acetoacetate

HRID 462462
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 462462
Cl[C:2]([CH2:4][O:5][CH2:6][C:7]([O:9][CH3:10])=[O:8])=[O:3].[CH3:11][C:12]1(C)[O:17]C(=O)[CH2:15][C:14](=O)[O:13]1.N1C=CC=CC=1>ClCCl>[CH3:10][O:9][C:7]([CH2:6][O:5][CH2:4][C:2](=[O:3])[CH2:11][C:12]([O:13][CH2:14][CH3:15])=[O:17])=[O:8]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 162492,2-Dimethyl-1,3-dioxane-4,6-dioneHCID 12361282Methyl (2-chloro-2-oxoethoxy)acetate

Produkt 1

HCID 13457217Ethyl 4-(methoxycarbonylmethoxy)acetoacetateAusbeute 12,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
5 °C

Versuchsvorschrift

Methyl 2-(chloroformylmethoxy)acetate (216.6 g) was added over 45 minutes to a stirred solution of 2,2-dimethyl-1,3-dioxane-4,6-dione (173.9 g) and pyridine (189.6 g) in dichloromethane (1000 ml) keeping the temperature below 5° C. The mixture was stirred at 5° C. for 30 minutes, allowed to warm up to room temperature over one hour, washed with 2.4M hydrochloric acid and water, dried over magnesium sulphate and evaporated. The resulting brown oil was dissolved in ethanol (300 ml) and the solution heated under reflux for 2.5 hours and evaporated. The residual oil was distilled to give the title compound (32.5 g), b.p. 138°-140°/1 torr which was characterised by its N.m.r. spectrum in CDCl3, δ values: 4.27 (2H,s); 4.20 (2H, q, J 7 Hz); 4.16 (2H,s); 3.75 (3H, s); 3.54 (2H, s); 1.29 (3H, t, J 7 Hz).

Aufarbeitung

  1. customthe temperature below 5° C
  2. temperatureto warm up to room temperature over one hour
  3. washwashed with 2.4M hydrochloric acid and water
  4. dry with materialdried over magnesium sulphate
  5. customevaporated
  6. dissolutionThe resulting brown oil was dissolved in ethanol (300 ml)
  7. temperaturethe solution heated
  8. temperatureunder reflux for 2.5 hours
  9. customevaporated
  10. distillationThe residual oil was distilled

Quellen und Nachweise

ORD-Eintrag
ord-96d5dc5cd7ea4545b5178e560b4f64b5
Quelldatensatz
uspto-grants-1985_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04515799

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