Water → HCID 178481862, Verbindung

Into 16.6 g (100.0 mmol) of 5-hydroxy-1-methyl-3-trifluoromethyl-1H-pyrazole in 15.4 g of N,N-dimethylformaldehyde was added 16.2 g (105.0 mmol) of phosphorus oxychloride at 0° C., followed by 1 hour of stirring at room temperature. Furthermore, the whole was stirred at 100° C. for 1 hour. After the completion of the reaction was confirmed, the reaction solution was poured into water and the pH was made 10 or more with a 25% sodium hydroxide solution and then the aqueous layer was washed with ethyl acetate. The pH of the resulting aqueous layer was made about 4 with a saturated citric acid solution and then extracted with diethyl ether. The resulting organic layer was washed with water and saline, successively, and then dried over anhydrous magnesium sulfate. The solvent was removed by evaporation under reduced pressure and the residue was purified by silica gel column chromatography to obtain 4.5 g (yield: 23.2%) of 5-hydroxy-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carbaldehyde.

1. stirringFurthermore, the whole was stirred at 100° C. for 1 hour
2. washmore with a 25% sodium hydroxide solution and then the aqueous layer was washed with ethyl acetate
3. extractionextracted with diethyl ether
4. washThe resulting organic layer was washed with water and saline
5. dry with materialsuccessively, and then dried over anhydrous magnesium sulfate
6. customThe solvent was removed by evaporation under reduced pressure
7. customthe residue was purified by silica gel column chromatography

ORD-Eintrag

ord-01ba60df1ee04fa3805d03bcbe4af0af

Quelldatensatz

uspto-grants-2007_08

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07256298B2