Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 474671Generated: October 31, 2026

Tetrahydrofuran → 2-[(4-Ethenylphenyl)oxy]-6-methylpyridine

https://huagongshe.com/reaction/474671

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant4-[(6-Methyl-2-pyridinyl)oxy]benzaldehydeHCID 86666211—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
Product2-[(4-Ethenylphenyl)oxy]-6-methylpyridineHCID 6777539751.1%

Reaction Steps

To a stirred suspension of 4-[(6-methyl-2-pyridinyl)oxy]benzaldehyde (2.43 g, 11.40 mmol) and methyl(triphenyl)phosphonium bromide (4.07 g, 11.40 mmol) in dry THF (30 mL) was added NaH (1.595 g, 39.9 mmol) under nitrogen at 0° C. The mixture was stirred at room temperature for 2 h. The organic layer was washed three times with brine, dried over Na2SO4, filtered, and concentrated. Purification via flash chromatography afforded the title compound (1.23 g, 5.82 mmol, 51.1% yield) as a light green oil. LCMS: rt=3.27 min, [M+H+]=212

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637536B2
Source datasetuspto-grants-2014_01
ORD IDord-57139d316ff641a189e2a1002e8821f3
Source noteuspto-grants-2014_01