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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 274824Generated: October 25, 2026

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

https://huagongshe.com/reaction/274824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHeptanoyl chlorideHCID 17313—
Reactant2-Decyl-5-(3-fluoro-4-hydroxyphenyl)pyrimidineHCID 15027167—
ReactantAceton-methanolHCID 21894497—
SolventPyridineHCID 1049—
Product2-Decyl-5-(3-fluoro-4-heptanoyloxyphenyl)pyrimidineHCID 1502716861.6%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05391318
Source datasetuspto-grants-1995_02
ORD IDord-6dd6ca04b52449b286ad6a2771e7457a
Source noteuspto-grants-1995_02