Potassium Hydroxide → 6-[(Methyloxy)carbonyl]-2-pyridinecarboxylate potassium salt

HRID 662096

Reaktionsgleichung

Reaktionsgleichung von HRID 662096
[N:1]1[C:6]([C:7]([O:9]C)=[O:8])=[CH:5][CH:4]=[CH:3][C:2]=1[C:11]([O:13][CH3:14])=[O:12].[OH-].[K+:16]>CO>[K+:16].[CH3:14][O:13][C:11]([C:2]1[N:1]=[C:6]([C:7]([O-:9])=[O:8])[CH:5]=[CH:4][CH:3]=1)=[O:12]

Komponenten

4

Edukt 2

HCID 14797Potassium HydroxideHCID 79549Dimethyl pyridine-2,6-carboxylate

Produkt 1

HCID 686324226-[(Methyloxy)carbonyl]-2-pyridinecarboxylate potassium saltAusbeute 79 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

To a suspension of dimethyl 2,6-pyridinedicarboxylate (95.22 g, 488 mmol) in a 2 L round-bottom flask under nitrogen in methanol (1,200 mL; ˜12.5 volumes) was added powdered potassium hydroxide (27.4 g, 488 mmol). The mixture was stirred and after 3 min was almost all in solution. After 20 min lab HPLC showed a 33:62 ratio of starting material to product. Solvent was evaporated and the resulting solid was stirred well with 1000 mL ethyl acetate, then filtered under vacuum, then dried at 40° C. under high vacuum to give 84.5 g (79%) of a white solid that lab HPLC showed to be 98.2% pure (ret time 1.41 min). LC-MS m/z 182 (M+H)+, 0.57 min (ret time).

Aufarbeitung

  1. waitAfter 20 min lab HPLC showed
  2. customSolvent was evaporated
  3. stirringthe resulting solid was stirred well with 1000 mL ethyl acetate
  4. filtrationfiltered under vacuum
  5. customdried at 40° C. under high vacuum

Quellen und Nachweise

ORD-Eintrag
ord-57ab9b8ca8b44f7bb1610342bd83a0a2
Quelldatensatz
uspto-grants-2011_12
Patentnummer
US08084449B2

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