HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-(3-Cyano-2-thienyl)benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2-(4-Methylphenyl)thiophene-3-carbonitrile | HCID 20092836 | — |
| Catalyst | Benzoyl Peroxide | HCID 7187 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 4-(3-Cyano-2-thienyl)benzyl bromide | HCID 20092857 | 40.9% |
Reaction Steps
24.5 g of 2-(4-methylphenyl)-3-cyanothiophene, prepared in E), are dissolved in 200 ml of carbon tetrachloride. 21.9 g of N-bromosuccinimide are added, as well as 0.1 g of benzoyl peroxide. The mixture is heated to reflux for 24 hours. The crystals of succinimide are filtered off and the solvent is evaporated off under vacuum. The residue is taken up in a mixture of hexane and ethyl acetate and the solution is kept in a freezer for 24 hours. The crystals formed are drained to give 14 g of 4-(3-cyano-2-thienyl)benzyl bromide in the form of crystals of melting point 80° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05358950 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-ed3c5c127f314628911976e96671415d |
| Source note | uspto-grants-1994_10 |