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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-Methoxybenzaldehyde | HCID 11569 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Methylpentane-2,3-dione 2-oxime | HCID 57357475 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 5-Isopropyl-2-(3-methoxyphenyl)-4-methyloxazole 3-oxide | HCID 57718886 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07825144B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-e532d802fa1846218c6c3e427608aab1 |
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| Source note | uspto-grants-2010_11 |
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