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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572673Generated: October 30, 2026

Potassium Carbonate → 2-Chloro-5-(5-oxazolyl)pyridine

https://huagongshe.com/reaction/572673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-Chloropyridine-3-carbaldehydeHCID 2764053—
ReactantToluenesulfonylmethyl isocyanideHCID 53627694—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product2-Chloro-5-(5-oxazolyl)pyridineHCID 2766284—

Reaction Steps

To a stirred suspension of 6-chloronicotinaldehyde (1.5 g, 10.59 mmol, Organic Letters 2005, 7(14) 2965-2967) and potassium carbonate (1.46 g, 10.5 mmol) in MeOH (50 mL) was added toluenesulphonylmethyl isocyanide (2.06 g, 10.59 mmol, Aldrich). The reaction mixture was heated to reflux for about 4 h. The reaction mixture diluted with water (50 mL) and the product was extracted with EtOAc (2×150 mL). The combined organic layers were washed successively with water (2×50 mL) and brine (1×50 mL), dried over sodium sulphate and evaporated to dryness. The crude material was purified by silica gel column chromatography eluted with 15% EtOAC in hexane. Relevant fractions containing the required compound were combined and evaporated to dryness under reduced pressure to afford 5-(6-chloropyridin-3-yl)oxazole as an off white solid 1.2 g (42.8. %), 1H NMR (400 MHz, CDCl3): δ 8.7 (d, J=2.0 Hz, 1H), 7.98 (s, 1H), 7.91 (d, J=2.4 Hz, 1H), 7.45 (s, 1H), 7.42 (d, J=8.4 Hz, 1H), MS m/z: 181 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029409B2
Source datasetuspto-grants-2015_05
ORD IDord-7805fadb6b634c9bb64dc1cba8ebb53f
Source noteuspto-grants-2015_05