HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylsilane → 4'-n-Pentyl-2,5-difluoro-4-bromobiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4'-Pentanoyl-2,5-difluoro-4-bromobiphenyl | HCID 14766052 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4'-n-Pentyl-2,5-difluoro-4-bromobiphenyl | HCID 14766053 | — |
Reaction Steps
Triethylsilane (7.0 g) is added dropwise over 2 h to a cooled, stirred (0° C.) solution of 1E (8.0 g) in trifluoroacetic acid (40 ml). The reaction mixture is stirred at room temperature overnight and poured into NaHCO3 solution. The product is extracted into ether twice and the combined ether layers are washed with water and dried (MgSO4). The solvent was removed in vacuo to yield an orange-brown oil. The crude product is distilled under reduced pressure (short path, 110°-120° C. at 0.01 mm Hg) to give a red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05273680 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-88e168a75b584d97b2f6ba639cfbe820 |
| Source note | uspto-grants-1993_12 |