3-(Trifluoromethyl)phenol → HCID 19044668, Verbindung

HRID 2400119Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2400119
[CH3:1][C:2]1[N:7]=[C:6](Cl)[C:5]([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:4][N:3]=1.[F:15][C:16]([F:25])([F:24])[C:17]1[CH:18]=[C:19]([OH:23])[CH:20]=[CH:21][CH:22]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O.CCOCC>[CH3:1][C:2]1[N:7]=[C:6]([O:23][C:19]2[CH:20]=[CH:21][CH:22]=[C:17]([C:16]([F:15])([F:24])[F:25])[CH:18]=2)[C:5]([CH2:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])=[CH:4][N:3]=1

Komponenten

6

Versuchsvorschrift

Ethyl α-(2-methyl-4-chloro-5-pyrimidinyl)-acetate (3 g, 14 mmol), 3-trifluoromethyl phenol (3 g, 14 mmol) and potassium carbonate (11 g, 80 mmol) in dimethylformamide (50 ml) are stirred at +80° C. for 3 hours. The mixture is diluted with ether and washed with brine. Drying over MgSO4 and evaporation of the solvent gives pure ethyl α-[2-methyl-4-(3-trifluoromethylphenoxy)-5-pyrimidinyl]acetate as an oil.

Aufarbeitung

  1. washwashed with brine
  2. dry with materialDrying over MgSO4 and evaporation of the solvent

Quellen und Nachweise

ORD-Eintrag
ord-cf2b357c89bc4f039a214ba864a9755e
Quelldatensatz
uspto-grants-1995_09
Patentnummer
US05453427

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