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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449422Generated: November 1, 2026

Water → (+)-5-Octyl-2-[4-(2-fluoroheptyloxy)phenyl]pyrimidine

https://huagongshe.com/reaction/1449422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant2-(4-Hydroxyphenyl)-5-octylpyrimidineHCID 604055—
Reactant(+)-2-Fluoroheptyl p-toluenesulfonateHCID 14716844—
Solvent1-ButanolHCID 263—
Product(+)-5-Octyl-2-[4-(2-fluoroheptyloxy)phenyl]pyrimidineHCID 1459723743%

Reaction Steps

IR (cm-1): 2900, 2850, 1600, 1450, 1350, 1170, 1090, 980, 810, 660, 550 0.43 g (1.5 mmol) of the thus obtained (+)-2-fluoroheptyl p-toluenesulfonate and 0.28 g (1.0 mmol) of 5-octyl-2-(4-hydroxyphenyl)pyrimidine were mixed with 0.2 ml of 1-butanol, followed by sufficient stirring. To the solution was quickly added a previously obtained alkaline solution of 0.048 g (1.2 mmol) of sodium hydroxide in 1.0 ml of 1-butanol, followed by 5.5 hours of heat-refluxing. After the reaction, 10 ml of distilled water was added, and the mixture was extracted respectively once with 10 ml of benzene and 5 ml of benzene, followed by drying with an appropriate amount of anhydrous sodium sulfate, distilling-off of the solvent and purification by silica gel column chromatography (chloroform) to obtain 0.17 g (0.43 mmol) of objective (+)-5-octyl-2-[4-(2-fluoroheptyloxy)phenyl]pyrimidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05599479
Source datasetuspto-grants-1997_02
ORD IDord-c8e045c0b52a4dc4944e1940b08ca944
Source noteuspto-grants-1997_02