HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 731927Generated: October 31, 2026
N-bromobutanimide → Ethyl 2-(bromomethyl)biphenyl-4-carboxylate
https://huagongshe.com/reaction/731927
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 2-methylbiphenyl-4-carboxylate | HCID 23112239 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Ethyl 2-(bromomethyl)biphenyl-4-carboxylate | HCID 23112214 | 758.3% |
Reaction Steps
In 130 ml of carbon tetrachloride was dissolved 10 g of ethyl 2-methylbiphenyl-4-carboxylate, the whole was heated to 90° C. and then 1.0 g of NBS and 136 mg of 2,2′-azobisisobutyronitrile were added thereto. After the reaction solution was heated under reflux, 6.78 g of NBS was added thereto and the whole was heated under reflux for 1 hour and a half. After the reaction solution was cooled to room temperature, precipitate was removed by filtration, water was added to the filtrate, and the organic layer was extracted with carbon tetrachloride. After the resulting organic layer was dried over anhydrous magnesium sulfate, the solvent was removed by evaporation to obtain 13.6 g of ethyl 2-(bromomethyl)biphenyl-4-carboxylate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07585878B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-145528f9e8a64739a3104fd160de4055 |
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| Source note | uspto-grants-2009_09 |
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