HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 20081759, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 20081760 | HCID 20081760 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20081759 | HCID 20081759 | 89.1% |
Reaction Steps
To a solution of the product of Step D (0.53 g, 1.38 mMol) in dry THF (10 mL) were added Ph3P (0.49 g, 2.06 mMol), CBr4 (0.69 g, 2.06 mMol) and CH3CN (2 mL), and the mixture was stirred at room temperature for 14 h. At the end of this period, the reaction mixture was concentrated in vacuo to provide an oil, which was then purified by flash chromatography on silica-gel using ethyl acetate-hexane (1:9) to provide the titled product as a thick colorless oil (0.57 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05401745 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-aebb1563b20f41a887624b1da83b429d |
| Source note | uspto-grants-1995_03 |