Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1780553Generated: October 26, 2026

Ethanol → 2-Fluoro-6-octyloxy3-(4-octyloxyphenyl)pyridine

https://huagongshe.com/reaction/1780553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactantp-Bromophenyl octyl etherHCID 145298—
Reactant2-Fluoro-6-octyloxypyridine-3-boronic acidHCID 19046940—
CatalystHCID 178418397HCID 178418397—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
Product2-Fluoro-6-octyloxy3-(4-octyloxyphenyl)pyridineHCID 1904696941.5%

Reaction Steps

2.00 g (7.44 mmol) of 2-fluoro-6-octyloxypyridine-3-boronic acid, 1.64 g (5.72 mmol) of 1-bromo-4-octyloxybenzene, 0.26 g (0.22 mmol) of tetrakis(triphenylphosphine)palladium(0) and 11.16 ml (22.32 mmol) of 2-molar sodium carbonate solution are refluxed in 20 ml of benzene and 10 ml of ethanol for 6 hours. After distributing the reaction mixture between water and diethyl ether, the organic phase is washed with water, dried over sodium sulfate, filtered and concentrated. Purification of the residue by chromatography (silica gel, 95:5 hexane/ethyl acetate) and recrystallization from acetonitrile give 1.02 g of 2-fluoro-6-octyloxy3-(4-octyloxyphenyl)pyridine. ##STR23##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05630962
Source datasetuspto-grants-1997_05
ORD IDord-dbb292851d0f40bdbc3c5e9e4eedc4a7
Source noteuspto-grants-1997_05