Carbon Dioxide → Methyl 4-methylthiazole-2-carboxylate

HRID 378837Notes

Reaction equation

HRID 378837 reaction equation
[CH3:1][C:2]1[N:3]=[CH:4][S:5][CH:6]=1.[CH2:7]([Li])CCC.[C:12](=[O:14])=[O:13]>O1CCCC1.CCCCCC>[CH3:1][C:2]1[N:3]=[C:4]([C:12]([O:14][CH3:7])=[O:13])[S:5][CH:6]=1

Participants

6

Conditions

Temperature
-78 °C

Procedure

To a solution of 4-methylthiazole (10 g) in anhydrous tetrahydrofuran (200 ml) was added n-butyl lithium in hexane (34.65 ml of 1.6M solution) dropwise at −78° C. The solution was stirred at −78° C. for 1 hour, at which point carbon dioxide gas was passed through the solution for 20 mins at −78° C. The solution was then allowed to warm to room temperature over 2 hours, the precipitate was filtered off, dissolved in methanol (200 ml) and added to methanolic hydrogen chloride (200 ml). The solution was stirred at room temperature overnight. The solvent was removed under vacuum and diethyl ether was added to the residue. The resultant solid was filtered off to yield the title compound as a white solid (2.2 g). 1H NMR (250 MHz, DMSO) δ 2.44 (3H, s), 3.89 (3H, s), 7.74 (1H, s).

Workup

  1. waitwas passed through the solution for 20 mins at −78° C
  2. temperatureto warm to room temperature over 2 hours
  3. filtrationthe precipitate was filtered off
  4. dissolutiondissolved in methanol (200 ml)
  5. additionadded to methanolic hydrogen chloride (200 ml)
  6. stirringThe solution was stirred at room temperature overnight
  7. customThe solvent was removed under vacuum and diethyl ether
  8. additionwas added to the residue
  9. filtrationThe resultant solid was filtered off

Sources & evidence

ORD record
ord-9f836ff1f4da4214ae2d6060d0754106
Source dataset
uspto-grants-2001_10
Patent number
US06297235B1

Reaction notes

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