HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 3-(2,2-Dibromoethenyl)-5-trimethylsilylfuran
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 5-(Trimethylsilyl)furan-3-carbaldehyde | HCID 15663251 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2,2-Dibromoethenyl)-5-trimethylsilylfuran | HCID 19991587 | — |
Reaction Steps
A solution of 2-trimethylsilyl-4-furaldehyde (Compound 4, 1.0 g, 5.95 mmol) in dichloromethane (2 ml) was added to a solution of triphenylphosphine (3.9 g, 14.9 mmol) and carbon tetrabromide 2.46 g, 7.44 mmol) in dichloromethane (15 ml) at 0° under argon. After 1 hour, the mixture was extracted thoroughly with pentane. Evaporation of the pentane extracts gave an oil, which was flash chromatographed on silica using hexane. Fractions with Rf of about 0.52 on evaporation gave the title silylfuran as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05013850 |
| Source dataset | uspto-grants-1991_05 |
| ORD ID | ord-e83e0ba68b2b450caa207ecec239906a |
| Source note | uspto-grants-1991_05 |