HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 6-Bromomethyl-2(2'-cyanophenyl)-naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 6-Methyl-2-(2'-cyanophenyl)-naphthalene | HCID 21848056 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 6-Bromomethyl-2(2'-cyanophenyl)-naphthalene | HCID 21848062 | — |
Reaction Steps
A mixture of 6.30 g of 6-methyl-2-(2'-cyanophenyl)-naphthalene, 4.60 g of N-bromosuccinimide and 0.085 g of azoisobutyronitrile in 70 ml of carbon tetrachloride is heated at 110° for 4 hours. The cooled reaction mixture is extracted twice with 45 ml of 2N sodium hydroxide solution each time. The aqueous phases are then extracted with 50 ml of CH2Cl in each case. The combined organic phases are dried over MgSO4. After removing the solvent in vacuo, the crude product is recrystallised from toluene/hexane and yields 6-bromomethyl-2-(2'-cyanophenyl)-naphthalene, m.p. 171-172°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05955487 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-77560c0366c446ad8eb8f75a9f146e5a |
| Source note | uspto-grants-1999_09 |