HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-Bromo-5-(bromomethyl)benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3-Bromo-5-methylbenzonitrile | HCID 14567858 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | 3-Bromo-5-(bromomethyl)benzonitrile | HCID 14567861 | 101% |
Reaction Steps
A mixture of 3-bromo-5-methylbenzonitrile (9.80 g, 45.0 mmol), NBS (8.90 g, 45.0 mmol) and BPO (0.40 g) in CCl4 (250 mL) was heated for 10 h at reflux. The reaction mixture was cooled to room temperature and filtered, and the organic phase was washed successively with saturated sodium bicarbonate (100 mL), water (2×50 mL) and brine (2×50 mL). The combined organic phases were dried over Na2SO4 and concentrated in vacuum to give 12.5 g of crude 3-bromo-5-(bromomethyl)benzonitrile.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071588B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-cd5557a76e354b5fab55d9b9ce7f7aa9 |
| Source note | uspto-grants-2011_12 |