Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503244Generated: October 30, 2026

6-Chloropyridine-3-carbaldehyde → HCID 117778379, compound

https://huagongshe.com/reaction/1503244

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloropyridine-3-carbaldehydeHCID 2764053—
ReactantPhosphonium, triphenyl[[4-(trifluoromethyl)phenyl]methyl]-, bromideHCID 10391293—
ReactantSodium t-butoxideHCID 23676156—
SolventEthanolHCID 702—
ProductHCID 117778379HCID 11777837925%

Reaction Steps

Triphenyl[4-(trifluoromethyl)benzyl]phosphonium bromide (6.4 g) and 6-chloropyridine-3-carboxaldehyde (1.8 g) were dissolved in ethanol (120 mL). To the solution, sodium tert-butoxide (1.2 g) was added at room temperature, and the mixture was stirred for 1 hour. The solvent was distilled off under reduced pressure, and ethyl acetate was added to the residue. The organic layer was washed with water and dried over sodium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (Yamazen Corporation, elution solvent: hexane/ethyl acetate). The obtained solid was washed with hexane to obtain the title compound (0.89 g) (yield: 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212170B2
Source datasetuspto-grants-2015_12
ORD IDord-00bab5032f7e4777b4b330a604dd6db0
Source noteuspto-grants-2015_12