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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038443Generated: November 1, 2026

Methanol → HCID 71060591, compound

https://huagongshe.com/reaction/1038443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPotassium CarbonateHCID 11430—
ReactantTosylmethyl isocyanideHCID 161915—
Reactant5-Fluoro-1H-indole-2-carbaldehydeHCID 18968129—
SolventHexaneHCID 8058—
ProductHCID 71060591HCID 7106059172%

Reaction Steps

To a 100 mL round-bottom flask was added 5-fluoro-1H-indole-2-carbaldehyde 47 (0.627 g, 3.84 mmol), methanol (40 mL), p-toluene sulfonylmethyl isocyanide (0.826 g, 4.23 mmol), followed by potassium carbonate (0.68 g, 4.92 mmol). The reaction mixture was stirred at reflux for about 1.5 hour and followed by TLC. The solvent was then evaporated and saturated aq. NaHCO3 was added. The resultant suspension was extracted with CH2Cl2 (2×20 mL). Combined organic layers were washed with brine, dried (anhydrous Na2SO4), and concentrated to leave a yellow solid. Crude product was further purified by silica-column chromatographed (Biotage) using Acetone:Hexane as an eluent to yield 5-(5-fluoro-1H-indol-2-yl)oxazole 48 (0.202 g, 72% yield). MS (ES) m/z 203 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551992B2
Source datasetuspto-grants-2013_10
ORD IDord-d747993b00214255a76f80af23eebdeb
Source noteuspto-grants-2013_10