HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1242395Generated: November 1, 2026
Azobisisobutyronitrile → 2-Bromomethyl-5-(4-trifluoromethyl-phenyl)-pyrimidine
https://huagongshe.com/reaction/1242395
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-Methyl-5-(4-trifluoromethyl-phenyl)-pyrimidine | HCID 21935946 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2-Bromomethyl-5-(4-trifluoromethyl-phenyl)-pyrimidine | HCID 21935922 | 35.2% |
Reaction Steps
0.31 g (1.3 mmol) of 2-methyl-5-(4-trifluoromethyl-phenyl)-pyrimidine, 0.255 g (1.43 mmol) of N-bromosuccinimide and 0.15 g (0.91 mmol) of 2,2′-azobis-(2-methyl-propionitril) were dissolved in 5 ml of carbon tetrachloride and the mixture was stirred at 75° C. Two portions of 0.13 g (0.73 mmol) of N-bromosuccinimide and of 0.075 g (0.046 mmol) of 2,2′-azobis-(2-methyl-propionitril) were added to the reaction mixture, after 4 and 8 hours, respectively, and heating was continued for additional 16 hours. After cooling to ambient temperature, the mixture was chromatographed on silicagel with dichloromethane as eluent. 0.145 g of the title compound was obtained as pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115611B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-453fe73909c1401b937444069e113c8c |
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| Source note | uspto-grants-2006_10 |
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