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Diethyl Malonate → HCID 20335826, Verbindung

HRID 2420476
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2420476
[C:1](OCC)(=O)CC(OCC)=O.[H-].[Na+].[C:14]([C:22]1[C:27]([N+:28]([O-:30])=[O:29])=[CH:26][CH:25]=[C:24](Cl)[N:23]=1)(=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>O1CCOCC1>[C:14]([C:22]1[C:27]([N+:28]([O-:30])=[O:29])=[CH:26][CH:25]=[C:24]([CH3:1])[N:23]=1)(=[O:21])[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 7761Diethyl MalonateHCID 24758Sodium hydrideHCID 20520021HCID 20520021, Verbindung

Produkt 1

HCID 20335826HCID 20335826, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 312751,4-DioxaneLösungsmittel

Versuchsvorschrift

They were added to a solution of 16.8 grams of diethyl malonate in 75 ml. of dioxane with stirring and under a nitrogen atmosphere 3.3 grams of sodium hydride (80%) and then stirring continued for 15 minutes more. Then there were added in portions 26.3 grams of 2-benzoyl-3-nitro-6-chloropyridine and then stirring was continued at 70° C. for two hours more. The precipitated deeply colored sodium salt of the dicarbethoxymethyl compound was filtered off with suction. Five grams of this compound were boiled under reflux in a mixture of 25 ml. of concentrated hydrochloric acid and 25 ml. of methanol for 90 minutes, the solution filtered hot and the filtrate treated with water to the point of turbidity. The desired product crystallized out.

Aufarbeitung

  1. stirringstirring
  2. waitwas continued at 70° C. for two hours
  3. customThe precipitated deeply colored sodium salt of the dicarbethoxymethyl compound
  4. filtrationwas filtered off with suction
  5. temperatureunder reflux in a mixture of 25 ml
  6. waitof methanol for 90 minutes
  7. filtrationthe solution filtered hot
  8. additionthe filtrate treated with water to the point of turbidity
  9. customThe desired product crystallized out

Quellen und Nachweise

ORD-Eintrag
ord-a35715f2261a46b39f331bf553a6a5d5
Quelldatensatz
uspto-grants-1978_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04110455

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