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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422152Generated: October 30, 2026

Acetone, oxime → 3-[2-(Diethyloxymethyl)-benzoyl]-2-[((isopropylidene)amino]oxy]-pyridine

https://huagongshe.com/reaction/1422152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetone, oximeHCID 67180—
Reactant(2-Fluoropyridin-3-yl)-2-(diethoxymethyl)-phenylmethanoneHCID 18357614—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
Product3-[2-(Diethyloxymethyl)-benzoyl]-2-[((isopropylidene)amino]oxy]-pyridineHCID 18357612—

Reaction Steps

To a solution of 0.49 g of acetone oxime in 8 ml of dry tetrahydrofuran was added 0.75 g of potassium tert-butoxide. The solution was stirred for 15 min. then a solution of 1.86 g of (2-fluoropyridin-3-yl)-2-(diethoxymethyl)-phenylmethanone in 8 ml of tetrahydrofuran was added. The solution was stirred at room temperature for 30 min. then quenched by the addition of 25 ml of a 1:1 water-saturated ammonium chloride solution. The solution was extracted with two 50 ml portions of ether and the combined ether extracts were washed with brine and dried over sodium sulfate. Evaporation afforded the intermediate 3-[2-(diethyloxymethyl)-benzoyl]-2-[((isopropylidene)amino]oxy]-pyridine which was not characterised but dissolved in 30 ml of ethanol and 20 ml of 2 M hydrochloric acid added and the solution refluxed for 15 min. The solution was cooled to room temperature and the crystals of 2-(isoxazolo[5,4-b]pyridin-3-yl)-benzaldehyde were collected by filtration and dried in vacuo, 1H-NMR (200 MHz, CDCl3) d 10.26 (CHO).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080773
Source datasetuspto-grants-2000_06
ORD IDord-669892d971a44b4bb04401f8121ceaae
Source noteuspto-grants-2000_06