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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225121Generated: October 26, 2026

Hydrochloric Acid → 2-Oximino-4-methyltetrahydro-1,4-oxazin-3-one

https://huagongshe.com/reaction/225121

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantIsobutyl nitriteHCID 10958—
Reactant4-Methylmorpholin-3-oneHCID 11007867—
ReactantPotassium tert-butoxideHCID 23665647—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product2-Oximino-4-methyltetrahydro-1,4-oxazin-3-oneHCID 86737353—

Reaction Steps

While maintaining the temperature near -55°, a solution of 11.5 grams of 4-methyltetrahydro-1,4-oxazin-3-one dissolved in 100 ml of anhydrous tetrahydrofuran was added over a period of twenty minutes to a slurry of 14.6 grams of potassium t-butoxide in 100 ml of tetrahydrofuran vigorously stirring under a nitrogen atmosphere. After equilibrating the resultant mixture for 30 minutes at -60°, a solution of 11.4 grams of isobutyl nitrite in 50 ml of tetrahydrofuran was added over 15 minutes while maintaining the temperature at -60° with external cooling. After a 15-minute equilibration at -60°, the reaction mixture was brought to 25° and stirred for 3 hours. The solution was then cooled to 0° and neutralized to pH 5 with 65 ml of a solution of 18 ml of conc. hydrochloric acid diluted to 100 mls. with absolute ethanol. After a 15-minute equilibration, potassium chloride was filtered off and the solvent removed in vacuuo. The resulting oil was triturated with 50 ml of ethyl acetate and the resulting solid was collected and then recrystallized from 150 ml. of acetonitrile yielding 5.07 g of the oxime product, mp. 199°-201°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04235902
Source datasetuspto-grants-1980_11
ORD IDord-2d6c36652e924e40ba78384408f7dd2d
Source noteuspto-grants-1980_11