Réaction #1273550

ord-369e6332ee8e427fae727406bbcd3553

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrereacted at room temperature for 2.2 hours
  2. 2
    AutreThen, purification by preparative thin-layer chromatography (chloroform/methanol=15/1)

Mode opératoire

According to Reference Example 8-2, by use of 4-methylthiazole-5-carbaldehyde (300 mg, 2.36 mmol) dissolved in N,N-dimethylformamide (4 mL), potassium carbonate (65 mg, 0.47 mmol) and (trifluoromethyl)trimethylsilane (0.419 mL, 2.83 mmol), the mixture was stirred and reacted at room temperature for 2.2 hours. Then, purification by preparative thin-layer chromatography (chloroform/methanol=15/1) was performed to give 2,2,2-trifluoro-1-(4-methylthiazol-5-yl)ethanol (Compound DT) (393 mg, yield: 84%).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08673908B2uspto-grants-2014_03