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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1503549Generated: October 29, 2026

Potassium Carbonate → N-(2-chloro-4-vinylbenzyl)pyridin-2-amine

https://huagongshe.com/reaction/1503549

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-4-((pyridin-2-ylamino)methyl)benzaldehydeHCID 86675182—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
Solvent1,4-DioxaneHCID 31275—
ProductN-(2-chloro-4-vinylbenzyl)pyridin-2-amineHCID 8667518350.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 3-chloro-4-((pyridin-2-ylamino)methyl)benzaldehyde (1 g, 4. mmol) in 1,4-dioxane (20 mL) were added K2CO3 (0.84 g, 6.09 mmol) and methyl triphenyl phosphonium bromide (2.17 g, 6.09 mmol) at ambient temperature. Then the resultant reaction mixture was heated at 100° C. for 18 h. After the reaction was deemed complete by TLC, the reaction mixture was cooled to ambient temperature and filtered, and the obtained filtrate was concentrated under reduced pressure. The residue was purified by flash chromatography (SiO2, 100-200 mesh; 10% EtOAc in n-Hexane) to afford the title compound as a white solid (0.5 g, 50%): mp 119-121° C.; 1H NMR (400 MHz, CDCl3) δ 8.12 (s, 1H), 7.42-7.40 (m, 3H), 7.26 (s, 1H), 6.66 (m, 2H), 6.36 (d, J=6.3 Hz, 1H), 5.75 (d, J=13.2 Hz, 1H), 4.92 (br s, 1H), 4.60 (s, 2H); ESIMS m/z 245.05 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212163B2
Source datasetuspto-grants-2015_12
ORD IDord-f51b43fd4c1f43009cd7f43231ac8743
Source noteuspto-grants-2015_12