HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-(bromomethyl)-6-methoxy-2-methyl-4-phenylisoquinolin-1(2H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 2,3-dimethyl-6-methoxy4-phenyl-2H-isoquinolin-1-one | HCID 22555991 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-(bromomethyl)-6-methoxy-2-methyl-4-phenylisoquinolin-1(2H)-one | HCID 22555947 | — |
Reaction Steps
To a solution of 12 (3.08 g, 11.0 mmol) in carbon tetrachloride under Argon was added N-bromosuccinimide (1.96 g, 11.0 mmol). The contents of the reaction flask were heated to reflux. After 3 h an additional portion of N-bromosuccinimide (0.50 g, 2.81 mmol) was added to the reaction flask. After 7 h the solvent was removed in vacuo and sat. sodium bicarbonate was added. Extracted with methylene chloride (4×) and dried the combined organic portions with magnesium sulfate (anh.). Removal of the solvent in vacuo followed by trituration with ether gave 13 as a light solid (3.47 g, 9.70 mmol, 88.2%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06870055B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-451ffba0cf3043e4ba1863900689913d |
| Source note | uspto-grants-2005_03 |