Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitroethane | HCID 6587 | — |
| Reactant | Phenyl isocyanate | HCID 7672 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-tert-Butylphenylacetylene | HCID 2757302 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57438911 | HCID 57438911 | — |
Reaction Steps
4.57 ml (42.12 mmol) of phenyl isocyanate are added dropwise at room temperature to a solution of 5 g (31.59 mmol) of 1-ethynyl-4-(tert-butyl)benzene, 0.75 ml (10.53 mmol) of nitroethane and 0.29 ml (2.10 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 9:1). 989 mg (14% of theory) of the title compound are obtained as a colorless 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-79c17ad90d444752a46ffa740914ea99 |
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| Source note | uspto-grants-2011_08 |
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