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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 274824Erstellt: 26. Oktober 2026

Heptanoyl chloride → 2-Decyl-5-(3-fluoro-4-heptanoyloxyphenyl)pyrimidine

https://huagongshe.com/reaction/274824

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHeptanoyl chlorideHCID 17313—
Edukt2-Decyl-5-(3-fluoro-4-hydroxyphenyl)pyrimidineHCID 15027167—
EduktAceton-methanolHCID 21894497—
LösungsmittelPyridineHCID 1049—
Produkt2-Decyl-5-(3-fluoro-4-heptanoyloxyphenyl)pyrimidineHCID 1502716861,6%

Reaktionsschritte

0.80 g (2.42 mmol) of 2-decyl-5-(3-fluoro-4-hydroxyphenyl) pyrimidine was dissolved in 10 ml of pyridine before 0.62 ml (4.00 mmol) of heptanoylchloride was added dropwise thereto while being cooled with ice and stirred. Then, the solution was cooled with ice and stirred for 15 minutes before it was heated and stirred for another 20 minutes in a water bath having a temperature maintained at 45° to 56° C. After the reaction had been completed, the solution was injected into 150 ml of ice water so as to filter and wash with water the deposited crystal. The thus obtained crystal was dissolved in toluene and the resultant toluene layer was washed with water and dried with dried mirabilite. The solvent was removed by lowering the pressure and distillation. The residue was purified by the silica gel column chromatography method which uses toluene as the eluate before it was recrystallized twice by an acetone-methanol mixed solvent so that 0.66 g (yield 61.6%) of 2-decyl-5-(3-fluoro-4-heptanoyloxyphenyl) pyrimidine was obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05391318
Quelldatensatzuspto-grants-1995_02
ORD IDord-6dd6ca04b52449b286ad6a2771e7457a
Quellennotizuspto-grants-1995_02