Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Camphor | HCID 2537 | — |
| Reactant | 3-Nitrobenzaldehyde | HCID 7449 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | Meta-nitrobenzylidenecamphor | HCID 67855246 | — |
Reaction Steps
The camphor (50.2 g, 0.33 mol), dimethoxyethane (180 ml) and sodium hydride (32 g at 50% in oil, 0.33 mol) washed with dimethoxyethane, are placed in a round-bottom flask. The mixture is heated under nitrogen to 80° C. and the meta-nitrobenzaldehyde (45.3 g, 0.3 mol) dissolved in dimethoxyethane (100 ml) is added dropwise over half an hour. The mixture is left stirring at 80° C. for 1.5 hours. The reaction mixture is allowed to cool and it is poured cautiously in 2 litres of acidified and ice cold water. The brown precipitate obtained is filtered, washed with water and dried. After recrystallisation in diisopropyl ether in the presence of vegetable black, 20 g of meta-nitrobenzylidenecamphor are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05236698 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-e51acbb4fd5d4f5890f24057daaa7743 |
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| Source note | uspto-grants-1993_08 |
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