HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156524Generated: October 25, 2026
Hydrochloric Acid → 5-[4-(Trifluoromethyl)phenyl]-1,2-oxazol-3-amine
https://huagongshe.com/reaction/1156524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | 3-Methoxy-2-propenenitrile | HCID 2723755 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3-(4-(Trifluoromethyl)phenyl)-3,3-dimethoxypropionitrile | HCID 20534839 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-[4-(Trifluoromethyl)phenyl]-1,2-oxazol-3-amine | HCID 13035545 | — |
Reaction Steps
3-(4-Trifluoromethyl)phenyl)-3-methoxyacrylonitrile plus 3-(4-(trifluoromethyl)phenyl)-3,3-dimethoxypropionitrile (1330 grams as a mixture) and hydroxylamine.HCl (1180 grams) were dissolved in methanol and chilled to 20° C. in an ice-bath. Next sodium methylate (1890 grams) was added portion-wise over a one and one-half hour period keeping the temperature between 20°-30° C. The reaction mixture was then heated to reflux for about 17 hours and then cooled to 40° C. and filtered. After the filtrate was stripped and poured into ice-water with stirring, a light yellow solid precipitate formed which was filtered and identified by NMR analysis as the desired product, yield 994 grams.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04336264 |
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| Source dataset | uspto-grants-1982_06 |
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| ORD ID | ord-cd164b732ae54991aca8bb08aabab14a |
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| Source note | uspto-grants-1982_06 |
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