Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 2-methyl-6-(trifluoromethyl)nicotinate | HCID 11564892 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 22600461 | HCID 22600461 | — |
Reaction Steps
434.4 g (1.866 mol) of ethyl 2-methyl-6trifluoromethylnicotinate (preparation similar to Heterocycles 129, 46, 1997) and 398.5 g (2.239 mol) of N-bromosuccinimide in 3 500 ml of carbon tetrachloride in the presence of 30.6 g (0.1866 mol) of α,α-azaisobutyronitrile are heated at 75° C., with irradiation from a 150 Watt lamp. After 3 hours, the reaction is terminated, the mixture is cooled to 15° C. and precipitated succinimide is removed by filtration. After evaporation of the solvent, the residue is distilled under reduced pressure. This gives ethyl 2-bromomethyl-6-trifluoromethylnicotinate as an oily product (260.2 g, 44.7% of theory, b.p. 74° C./0.04 mmHg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06838564B2 |
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| Source dataset | uspto-grants-2005_01 |
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| ORD ID | ord-eb5e45ca00d6437fbb96738c3fdfca50 |
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| Source note | uspto-grants-2005_01 |
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