HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tributylstannane → 1-Bromo-2-(2,2,2-trifluoroethyl)benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Imidazole-1-carbothioic acid O-[1-(2-bromophenyl)-2,2,2-trifluoroethyl]-ester | HCID 57582364 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-Bromo-2-(2,2,2-trifluoroethyl)benzene | HCID 45790473 | 96.4% |
Reaction Steps
A solution of imidazole-1-carbothioic acid O-[1-(2-bromophenyl)-2,2,2-trifluoroethyl]-ester (Preparation 56, 27.0 g, 73.8 mmol) in toluene (400 ml) was heated at reflux and treated with tri-n-butyltin hydride in three portions: 22 g (75.6 mmol) at first, an additional 10 g (34.4 mmol) after 30 min, and finally 11 g (37.8 mmol) 30 min later. After the addition, the mixture was heated at reflux for another 30 min. The reaction mixture was cooled then the product was distilled at 25 Pa, 60-100° C. to afford the title compound as a colourless oil (17.0 g, 59%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08134007B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-7b92846416f54a358a6c43e185f2430a |
| Source note | uspto-grants-2012_03 |