HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35989Generated: October 26, 2026
Hydrochloric Acid → (4-Bromophenyl)(4-fluorophenyl)methanone
https://huagongshe.com/reaction/35989
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Fluorobenzene | HCID 10008 | — |
| Reactant | 4-Bromobenzoyl chloride | HCID 68515 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | (4-Bromophenyl)(4-fluorophenyl)methanone | HCID 74951 | 86% |
Reaction Steps
In a 250 mL flask equipped with a nitrogen inlet, overhead stirring assembly, and reflux condenser were placed fluorobenzene (117 g, 1.2 mol) and 4-bromobenzoyl chloride (39.8 g, 0.181 mol). The mixture was cooled to 0° C. and aluminum chloride (27 g, 0.20 mol) was added. The mixture was stirred for 15 minutes at 23° C., followed by heating to reflux for 4 h. The reaction was then cooled to 23° C. and stirred for 16 h. The resulting slurry was poured into 2 L of acidic (HCl) water. The organics were extracted with methylene chloride, and dried over magnesium sulfate. The slurry was filtered and the methylene chloride was removed under reduced pressure to yield an off white powder. Recrystallization from ethanol afforded 43.3 g (86%) of 4-bromo-4'-fluorobenzophenone as white crystals: m.p. 106°-107° C., (Lit. 107°-108° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05412066 |
|---|
| Source dataset | uspto-grants-1995_05 |
|---|
| ORD ID | ord-52ddc66d1eb0405192a178ae86bfd4f9 |
|---|
| Source note | uspto-grants-1995_05 |
|---|