HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669800Generated: October 31, 2026
Nitroethane → 3-Methyl-5-(4-methylphenyl)isoxazole
https://huagongshe.com/reaction/1669800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitroethane | HCID 6587 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | p-Ethynyltoluene | HCID 13018 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Methyl-5-(4-methylphenyl)isoxazole | HCID 10352172 | — |
Reaction Steps
6.23 ml (57.39 mmol) of phenyl isocyanate are added dropwise at room temperature to a solution of 5 g (43.04 mmol) of 1-ethynyl-4-methylbenzene, 1 ml (14.34 mmol) of nitroethane and 0.4 ml (2.87 mmol) of triethylamine in 100 ml of benzene. The reaction mixture is then stirred under reflux for 12 h. After cooling, the suspension is mixed with water (50 ml) and stirred at room temperature for a further 4 h. The precipitate is filtered off with suction and washed with benzene (10 ml). The organic phase of the filtrate is separated off, dried with magnesium sulfate and concentrated. The residue is purified by column chromatography on silica gel (mobile phase: cyclohexane/ethyl acetate 6:1). 1.13 g (46% of theory) of the title compound are obtained as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989633B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-c18b0c05541743429217e7dd1b28c986 |
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| Source note | uspto-grants-2011_08 |
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