HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → 4-Octyl-2'-fluoro-4'-bromobiphenyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 4-Octanoyl-2'-fluoro-4'-bromobiphenyl | HCID 18985426 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Octyl-2'-fluoro-4'-bromobiphenyl | HCID 14766292 | 71.1% |
Reaction Steps
In a reactor were placed 3.75 g of 4-octanoyl-2'-fluoro-4'-bromobiphenyl and 20 ml of trifluroacetic acid, to which was added 2.4 g of triethylsilane at room temperature and stirred for 6 hours. Then, the reaction solution was added into water, extracted into benzene, washed sequentially with water, aqueous sodium hydrogencarbonate, and again water, and dehydrated over Glauber's salt. After the solvent was distilled off, the residue was evaporated in a glass tube oven (GTO) to obtain 2.56 g of 4-octyl-2'-fluoro-4'-bromobiphenyl (71.1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05271867 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-2217cc47ec4d4b8f847a904bcca84492 |
| Source note | uspto-grants-1993_12 |