HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010834Generated: October 31, 2026
Ethanol → 5-Amino-3-phenyl-1,2-oxazole-4-carbonitrile
https://huagongshe.com/reaction/1010834
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 2-(Ethoxy-phenyl-methylene)-malononitrile | HCID 2786701 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Amino-3-phenyl-1,2-oxazole-4-carbonitrile | HCID 13449567 | — |
Reaction Steps
Hydroxylamine hydrochloride was suspended in water (30 ml) and sodium hydroxide (4.4 g, 0.11 mole) and then ethanol (40 ml) was added, followed by batchwise addition of 2-(ethoxy-phenyl-methylene)-malononitrile (21.7 g, 0.11 mole). The reaction mixture was heated to 50° C. for 2 hours. The ethanol was removed under vacuum and the precipitate was filtered. The precipitate was redissolved in 50% ethyl acetate/hexanes and chromatographed on silica gel to give 8.2 g of product after removal of solvent (yield: 40%). The rest of the sequence was made by analogy to the methyl replacement of the phenyl analog.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07977342B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-1aa0bc934e8b447482546ca474dd12f9 |
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| Source note | uspto-grants-2011_07 |
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