Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 2,3-Dihydro-1H-indene-2-carbonitrile | HCID 23239618 | — |
| Solvent | Acetic Anhydride | HCID 7918 | — |
| Product | 2-Cyano-5-nitroindane | HCID 18958962 | 81% |
Reaction Steps
Fuming nitric acid (40 ml, 1.5 g/ml) was added dropwise with stirring to acetic anhydride (80 ml ) keeping the temperature of the mixture at 0° C. After the addition was complete 2-cyanoindane (11.33 g, 79.5 mmol), (J. Chem. Soc. (B), (1969), 1197) was added dropwise with stirring over 30 minutes maintaining the reaction temperature between -5° and 0° C. The mixture was stirred for a further 15 minutes then poured onto ice. The mixture was extracted with dichloromethane (4×150 ml) and the extracts were washed with saturated aqueous sodium bicarbonate (3×150 ml), dried over magnesium sulphate and the solvent evaporated under reduced pressure. The residue was recrystallised from ethanol to give 2-cyano-5-nitroindane (12.09 g, 81%) as a yellow solid, m.p. 80°-82° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05358953 |
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| Source dataset | uspto-grants-1994_10 |
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| ORD ID | ord-d98ba50076f94851a87b012e7c1c7191 |
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| Source note | uspto-grants-1994_10 |
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