HuagongsheHuagongshe Chemistry Print Report · For research reference only
Boron trifluoride → [4-(4-Fluorobenzoyl)phenyl]-(4-fluorophenyl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | Terephthaloyl chloride | HCID 7488 | — |
| Reactant | Fluorobenzene | HCID 10008 | — |
| Reactant | Hydrofluoric Acid | HCID 14917 | — |
| Product | [4-(4-Fluorobenzoyl)phenyl]-(4-fluorophenyl)methanone | HCID 11141804 | 122.6% |
Reaction Steps
20.3 g of terephthaloyl dichloride, 19.2 g of fluorobenzene and 50 g of hydrogen fluoride were initially introduced into a 250 ml stainless steel autoclave and boron trifluoride was introduced under pressure at 10 bar. The autoclave was shaken for 16.5 h at room temperature. Working-up was carried out by initially evaporating the volatile components at room temperature and then at 60° to 100° C. and recrystallizing the residue from chlorobenzene in the presence of sodium carbonate. 19.76 g of 1,4-bis-(4-fluorobenzoyl)-benzene were obtained in the form of colorless crystals of m.p. 221° C. Examination by means of high pressure liquid chromatography (HPLC) gave a degree of purity of 99.5%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04924014 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-02cb75b589704f51b7d314d24a3b86e8 |
| Source note | uspto-grants-1990_05 |