Carbon Dioxide → 1-Methyl-1H-1,2,4-triazole-5-carboxylic acid

HRID 244633Notes

Reaction equation

HRID 244633 reaction equation
[CH3:1][N:2]1[CH:6]=[N:5][CH:4]=[N:3]1.C([Li])CCC.[C:12](=[O:14])=[O:13]>C1COCC1.CCCCCC>[CH3:1][N:2]1[C:6]([C:12]([OH:14])=[O:13])=[N:5][CH:4]=[N:3]1

Participants

6

Conditions

Temperature
-78 °C

Procedure

1-Methyl-1H-1,2,4-triazole (1.19 g) was dissolved in THF (15 ml) and cooled to −78° C. under nitrogen. A 1.6M solution of butyllithium in hexane (9.4 ml) was added dropwise. The solution was stirred for 1.5 h at −78° C., then the solution was treated with solid carbon dioxide (2 g). After 30 min at −78° C. the solution was allowed to warm to RT and stirred overnight. The reaction was quenched with water (1 ml) and the solvent was decanted off. To the residue was added ethyl acetate (20 ml) and water (20 ml). The solvent was removed in vacuo and the residue was dried in a vacuum oven for 1 day (50° C.) to give the title compound (1.61 g) as a white solid.

Workup

  1. waitAfter 30 min at −78° C. the solution was allowed
  2. temperatureto warm to RT
  3. stirringstirred overnight
  4. customThe reaction was quenched with water (1 ml)
  5. customthe solvent was decanted off
  6. additionTo the residue was added ethyl acetate (20 ml) and water (20 ml)
  7. customThe solvent was removed in vacuo
  8. customthe residue was dried in a vacuum oven for 1 day (50° C.)

Sources & evidence

ORD record
ord-26fa0ad4425742879cadda3a95cacd2a
Source dataset
uspto-grants-2014_02
Patent number
US08658635B2

Reaction notes

Loading…