HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-(Bromomethyl)naphthalene-1-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1-Cyano-4-methylnaphthalene | HCID 142047 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(Bromomethyl)naphthalene-1-carbonitrile | HCID 12433008 | 74.7% |
Reaction Steps
2.50 g (14.95 mmol) of 4-methyl-1-naphthonitrile are dissolved in 40 ml of tetrachloromethane and 3.19 g (17.94 mmol) of N-bromosuccinimide and 245 mg (1.50 mmol) of 2,2′-azobis-2-methylpropanenitrile are added. The mixture is stirred at the reflux temperature overnight. After cooling, the product is filtered off. 2.75 g (74.7% of theory) of 4-(bromomethyl)-1-naphthonitrile are obtained in a purity of 90% and are reacted without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09051316B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-a0a03cfcb4084e07ac63ec4db668bdbd |
| Source note | uspto-grants-2015_06 |