Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 8-Nitroquinoline | HCID 11830 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Iodo-8-nitroquinoline | HCID 12032367 | 98.2% |
Reaction Steps
A stirred mixture of 8-nitroquinoline (100 g, 0.57 mol) in acetic acid (500 ml) was treated with N-iodosuccinimide (155 g, 0.69 mol) portionwise over 10 minutes, and warmed to 62° C. for 6 h. A further portion of N-iodosuccinimide (25 g, 0.14 mol) was introduced and the mixture stirred for a further 16 h before cooling to ambient temperature. The solvent was removed in vacuo, keeping the temperature below 35° C. The residue was dissolved in dichloromethane (2 L) and washed successively with saturated aqueous sodium bicarbonate solution (2×1 L), 10% aqueous sodium thiosulphate solution (1 L), water (1 L), brine (100 ml), then the organic phase was dried over magnesium sulphate. The mixture was filtered and the solvent removed to give a yellow solid which was recrystallised from ethyl acetate to give the title compound (D3) (168 g, 97%) as a yellow solid;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799774B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-1efc24cc7936423286248d3e44073169 |
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| Source note | uspto-grants-2010_09 |
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