HuagongsheHuagongshe Chemistry Print Report · For research reference only
Azobisisobutyronitrile → Ethyl 3'-(bromomethyl)biphenyl-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Azobisisobutyronitrile | HCID 6547 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4'-Bromomethyl-biphenyl-3-carboxylic acid ethyl ester | HCID 21464255 | — |
| Reactant | 3'-Methyl-biphenyl-3-carboxylic acid ethyl ester | HCID 58610589 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Ethyl 3'-(bromomethyl)biphenyl-3-carboxylate | HCID 58610582 | — |
Reaction Steps
3′-Bromomethyl-biphenyl-3-carboxylic acid ethyl ester was synthesized as described for 4′-bromomethyl-biphenyl-3-carboxylic acid ethyl ester. 3′-Methyl-biphenyl-3-carboxylic acid ethyl ester (4.2 g, 17.48 mmol, 1 eq.) in carbon tetrachloride was treated with N-bromosuccinimide (3.73 g, 20.98 mmol, 1.2 eq.) and 2,2′-azobisisobutyronitrile (0.14 g, 0.87 mmol, 5 mol %). When complete, the reaction was worked up as described leaving an orange oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132456B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-a57d8b08ddea457495105a5b1b3b4d89 |
| Source note | uspto-grants-2006_11 |