HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 3-(Bromomethyl)thiophene-2-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Cyano-3-hydroxymethylthiophene | HCID 21866490 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(Bromomethyl)thiophene-2-carbonitrile | HCID 13553081 | 110.7% |
Reaction Steps
11.7 g (84.07 mmol) of 2-cyano-3-hydroxymethylthiophene were dissolved together with 24.1 g (91.87 mmol) of triphenylphosphine in 100 ml of THF at room temperature and, while cooling (ice bath), 30.47 g (91.87 mmol) of tetrabromomethane were added in portions. Stirring at room temperature for 3 hours was followed by concentration under reduced pressure and purification by chromatography on silica gel (methylene chloride/petroleum ether) to result in 18.8 g of pale yellow crystalline product still containing petroleum ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06114358 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-b32d28022c9e48baae1e8c8dfc583868 |
| Source note | uspto-grants-2000_09 |