Réaction #2487394

ord-10dda8e7e6f34753b941450150cc9cb4

Équation de réaction

[Al+3].[H-].[H-].[H-].[H-].[Li+]
lithium aluminum hydride
O=C(O)c1cccnc1O
2-hydroxynicotinic acid
O=c1[nH]cccc1CO
3-hydroxymethyl-2-pyridone
Rendement 32.4%

Conditions de réaction

Température
0°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrereturned to room temperature
  2. 2
    Températurebefore being refluxed for 8 h
  3. 3
    TempératureThe reaction was cooled to room temperature
  4. 4
    Autrewas quenched with 1.6 mL of water, 1.6 mL of 15% NaOH
  5. 5
    AutreThe solvent was removed in vacuo
  6. 6
    FiltrationThe solution was filtered through celite
  7. 7
    Autrethe solvent removed in vacuo

Mode opératoire

In Example 1, 1.6063 g (42.33 mmol) of lithium aluminum hydride (LAH) was suspended in 100 mL of tetrahydrofuran (THF) in a 250 mL round bottom flask (RBF) under the presence of argon gas (99.999% purity) and was cooled to 0° C. in an ice bath. 5.0946 g (36.62 mmol) of 2-hydroxynicotinic acid was slowly added, and the solution returned to room temperature before being refluxed for 8 h. The reaction was cooled to room temperature and was quenched with 1.6 mL of water, 1.6 mL of 15% NaOH and an additional 4.8 mL of water. The solvent was removed in vacuo and the residue was taken up in 100 mL of refluxing ethanol. The solution was filtered through celite and the solvent removed in vacuo to produce 1.4848 g (32.40% yield) of 3-hydroxymethyl-2-pyridone. Characterization data of the product was consistent with literature.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08795630B2uspto-grants-2014_08