Carbon Tetrachloride → Methyl 2-methoxypyridine-3-carboxylate

HRID 66587Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 66587
S(Cl)(Cl)=O.[CH3:5][O:6][C:7]1[C:12]([C:13]([OH:15])=[O:14])=[CH:11][CH:10]=[CH:9][N:8]=1.[C:16](Cl)(Cl)(Cl)Cl>>[CH3:5][O:6][C:7]1[C:12]([C:13]([O:15][CH3:16])=[O:14])=[CH:11][CH:10]=[CH:9][N:8]=1

Komponenten

4

Edukt 3

HCID 5943Carbon TetrachlorideHCID 24386Thionyl ChlorideHCID 7080932-Methoxynicotinic acid

Produkt 1

HCID 10820973Methyl 2-methoxypyridine-3-carboxylate

Versuchsvorschrift

Thionyl chloride (50 ml.) was added to 2-methoxypyridine-3-carboxylic acid (5 g.) in 50 ml. of carbon tetrachloride and the mixture refluxed for 2 hours. The reaction mixture was cooled, evaporated to solids and chased with multiple portions of fresh carbon tetrachloride. The resulting acid chloride hydrochloride was dissolved in excess methanol (50 ml.), stirred for 16 hours at room temperature, then evaporated an oil and taken up in chloroform. The chloroform solution was washed with two portions of saturated sodium bicarbonate and then one portion of brine, dried over anhydrous magnesium sulfate, filtered and evaporated to yield title product as an oil [4.63 g.; pnmr/CDCl3 /delta (ppm): 3.9 and 4.1 (2s, 6H), 6.9 (m, 1H), 8.2 (m, 2H)].

Aufarbeitung

  1. temperatureThe reaction mixture was cooled
  2. customevaporated to solids and chased with multiple portions of fresh carbon tetrachloride
  3. dissolutionThe resulting acid chloride hydrochloride was dissolved in excess methanol (50 ml.)
  4. customevaporated an oil
  5. washThe chloroform solution was washed with two portions of saturated sodium bicarbonate
  6. dry with materialone portion of brine, dried over anhydrous magnesium sulfate
  7. filtrationfiltered
  8. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-512d46fcf226412c9f7207cff92f9cda
Quelldatensatz
uspto-grants-1982_08
Patentnummer
US04342771

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