HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyano-3-methylisoquinoline → 3-(Bromomethyl)-4-isoquinolinecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyano-3-methylisoquinoline | HCID 1733 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-(Bromomethyl)-4-isoquinolinecarbonitrile | HCID 57499772 | — |
Reaction Steps
39 mg azo-isobutyronitrile are added to a boiling mixture of 400 mg 3-methyl-4-cyano-isoquinoline and 440 mg N-bromosuccinimide in 30 ml carbon tetrachloride. The reaction mixture is refluxed for two hours. After cooling to ambient temperature the precipitate formed is suction filtered and washed with carbon tetrachloride. The filtrate is evaporated down and chromatographed through a silica gel column with methylene chloride as eluant.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07495002B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-f7a5864a6eba44459338f66efb97bc74 |
| Source note | uspto-grants-2009_02 |