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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1169822Generated: October 31, 2026

Hydrochloric Acid → 5-Isopropyl-2-(3-methoxyphenyl)-4-methyloxazole 3-oxide

https://huagongshe.com/reaction/1169822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-MethoxybenzaldehydeHCID 11569—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Methylpentane-2,3-dione 2-oximeHCID 57357475—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Solventtert-Butyl methyl etherHCID 15413—
Product5-Isopropyl-2-(3-methoxyphenyl)-4-methyloxazole 3-oxideHCID 57718886—

Reaction Conditions

Temperature52.5 °C

Reaction Steps

19.0 g (137 mmol) of 3-methoxybenzaldehyde were added to a solution of 18.0 g (137 mmol) of 4-methylpentane-2,3-dione 2-oxime in 30 g (99 mmol) of solution of hydrogen chloride in acetic acid (12%) and 30 g (164 mmol) of solution of hydrogen chloride in ethylene glycol dimethyl ether (20%). The reaction was stirred at 50-55° C. for 3 hours and at room temperature for 60 hours. Subsequently, 500 ml of water and 300 ml of tert-butyl methyl ether were added before a pH of 3-4 was established by adding sodium hydrogen carbonate. After phase separation, the aqueous phase was extracted twice with 100 ml each time of tert-butyl methyl ether. The combined organic phases were washed with 4×100 ml of water and concentrated fully under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07825144B2
Source datasetuspto-grants-2010_11
ORD IDord-e532d802fa1846218c6c3e427608aab1
Source noteuspto-grants-2010_11