HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395203Generated: October 26, 2026
Azobisisobutyronitrile → Methyl 2-bromo-2-[3-(trifluoromethyl)phenyl]acetate
https://huagongshe.com/reaction/1395203
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl (3-(trifluoromethyl)phenyl)acetate | HCID 2734603 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl 2-bromo-2-[3-(trifluoromethyl)phenyl]acetate | HCID 19796654 | — |
Reaction Steps
To the solution of 21.8 g of methyl m-trifluoromethylphenylacetate in 450 ml of carbon tetrachloride a portion of 18.7 g of N-bromosuccinimide is added along with several drops of triethylamine and a pinch of azobisisobutyronitrile. The mixture is warmed to reflux with a 250 watt incandescent bulb and a precipitate is formed. Thereupon the remainder of N-bromosuccinimide is added, the light removed and the solution stirred for 3 hours. It is cooled in an ice bath and the solid formed removed by filtration. The filtrate is evaporated the residue dissolved in diethyl ether-water and the organic phase washed with aqueous sodium bicarbonate and water. It is dried, evaporated, the residue distilled and the fraction boiling at 85°-88°/0.4 mmHg collected, to yield the methyl α-bromo-m-trifluoromethylphenylacetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04202901 |
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| Source dataset | uspto-grants-1980_05 |
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| ORD ID | ord-25fba002a98342d2b24f3af449f3b392 |
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| Source note | uspto-grants-1980_05 |
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