Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572674Generated: October 31, 2026

Potassium Carbonate → 5-broMo-2-(1,3-oxazol-5-yl)pyridine

https://huagongshe.com/reaction/572674

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromopyridine-2-carbaldehydeHCID 9877562—
ReactantToluenesulfonylmethyl isocyanideHCID 53627694—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product5-broMo-2-(1,3-oxazol-5-yl)pyridineHCID 23438598—

Reaction Steps

To a stirred suspension of 5-bromopicolinaldehyde (0.412 g, 2.215 mmol, Tetrahedron Letters 2008, 64, 3794-3801) and potassium carbonate (0.3358 g, 2.43 mmol, Rankem) in MeOH (20 mL) was added toluenesulphonylmethyl isocyanide (0.4757 g, 2.43 mmol). The reaction mixture was heated to reflux for about 4 h. The reaction mixture diluted with water (100 mL) and the product was extracted with EtOAc (2×75 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 obtained was purified by silica gel column chromatography eluted with 10% EtOAC in hexane. Relevant fractions containing the target compound were combined and evaporated to dryness under reduced pressure to afford 5-(5-bromopyridin-2-yl)oxazole as an off white solid 0.35 g (70.2%), 1H NMR (400 MHz, DMSO): δ 8.7 (d, J=2.4 Hz, 1H), 8.57 (s, 1H), 8.2 (dd, J=8.4 Hz, 1H), 7.8 (s, 1H), 7.7 (d, J=8.8 Hz, 1H), MS m/z: 226 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029409B2
Source datasetuspto-grants-2015_05
ORD IDord-4fc3bc5c3d2d4701864144bfaf4736d4
Source noteuspto-grants-2015_05