HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 2'-Bromomethyl-biphenyl-4-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2'-Methylbiphenyl-4-carboxylic acid ethyl ester | HCID 12171893 | — |
| Reactant | 4'-Bromomethyl-biphenyl-3-carboxylic acid ethyl ester | HCID 21464255 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 2'-Bromomethyl-biphenyl-4-carboxylic acid ethyl ester | HCID 21999240 | 99% |
Reaction Steps
2′-Bromomethyl-biphenyl4-carboxylic acid ethyl ester was synthesized as described for 4′-bromomethyl-biphenyl-3-carboxylic acid ethyl ester. 2′-Methyl-biphenyl-4-carboxylic acid ethyl ester (4.4 g, 18.31 mmol, 1 eq.) in carbon tetrachloride was treated with N-bromosuccinimide (3.58 g, 20.14 mmol, 1.1 eq.), and 2,2′-azobisisobutyronitrile (0.15 g, 0.92 mmol, 5 mol %). When complete, the reaction was worked up as described leaving 2′-bromomethyl-biphenyl-4-carboxylic acid ethyl ester (5.77 g, 99% yield) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07132456B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-41d7aa59ad0945c0afdc1468984c3bc6 |
| Source note | uspto-grants-2006_11 |