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Methanol → Methyl 3-methylpyrazine-2-carboxylate

HRID 627701
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 627701
[CH3:1][C:2]1[C:3]([C:8]([OH:10])=[O:9])=[N:4][CH:5]=[CH:6][N:7]=1.S(=O)(=O)(O)O.[CH3:16]O>>[CH3:1][C:2]1[C:3]([C:8]([O:10][CH3:16])=[O:9])=[N:4][CH:5]=[CH:6][N:7]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 3

HCID 887MethanolHCID 1118Sulfuric AcidHCID 131534683-Methylpyrazine-2-carboxylic acid

Produkt 1

HCID 13153469Methyl 3-methylpyrazine-2-carboxylateAusbeute 73 %

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

In a 2-L flask, 3-methylpyrazine-2-carboxylic acid (Matrix, 19.95 g, 144 mmol) was suspended in MeOH (500 mL). The suspension was cooled in an ice-water bath, and concentrated sulfuric acid (Fluka, 27.3 mL, 506 mmol) was added over a time period of 5 min. The reaction mixture was heated to 80° C. for 5 h. The reaction mixture was concentrated under reduced pressure and the residue was taken up in DCM (750 mL). The excess acid was neutralized carefully with aqueous NaOH (5M, 200 mL). The aqueous layer was separated and extracted with DCM (250 mL). The combined organic layers were combined, dried over MgSO4 and concentrated to afford the title compound (16.15 g, 106 mmol, 73%). MS m/z=153 (M+H).

Aufarbeitung

  1. temperatureThe suspension was cooled in an ice-water bath
  2. concentrationThe reaction mixture was concentrated under reduced pressure
  3. customThe aqueous layer was separated
  4. extractionextracted with DCM (250 mL)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-a33485ce69e04e7b9101871c7b8aa1b3
Quelldatensatz
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09309263B2

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