HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloride → 2-Triethylsilyl-5-phenyl-4-furaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Phenyl Trifluoromethanesulfonate | HCID 548641 | — |
| Reactant | 3-Furancarboxaldehyde, 5-(triethylsilyl)- | HCID 10878438 | — |
| Reactant | HCID 178506926 | HCID 178506926 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Product | 2-Triethylsilyl-5-phenyl-4-furaldehyde | HCID 19433144 | — |
Reaction Steps
Treatment of 2-triethylsilyl-4-furaldehyde with lithio N,N,N'-trimethylethylenediamine, followed by phenyl trifluoromethanesulfonate in the presence of anhydrous zinz chloride and tetrakis (triphenylphosphine) palladium (o) and work up gives the titled aldehyde.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05322953 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-33be0630a2914d0ba4116713fa7cfd47 |
| Source note | uspto-grants-1994_06 |