HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Methyl 4'-(bromomethyl)biphenyl-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | (1,1'-Biphenyl)-2-carboxylic acid, 4'-methyl-, methyl ester | HCID 1393873 | — |
| Catalyst | Azobisisobutyronitrile | HCID 6547 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | Methyl 4'-(bromomethyl)biphenyl-2-carboxylate | HCID 11012181 | 86.9% |
Reaction Steps
N-Bromosuccinimide (8.1 g) and azo(bisisobutyronitrile) (130 mg) were added to a solution of compound (B1) (9.3 g) in carbon tetrachloride (300 ml). The mixture was heated under reflux for 4 hours and then cooled to ambient temperature. Insoluble material was removed by filtration and the filtrate concentrated. The residue was purified by flash chromatography, eluting with ethyl acetate/hexane (1:9 v/v) to give methyl 4'-(bromomethyl)biphenyl-2-carboxylate (C1) as a solid (10.9 g), m.p. 48°-50° C.; NMR: 3.65(s,3H), 4.55(s,2H), 7.25-7.60 (complex m,7H), 7.85(d,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05126344 |
| Source dataset | uspto-grants-1992_06 |
| ORD ID | ord-61973961178c4d1781b1387138669af8 |
| Source note | uspto-grants-1992_06 |