HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzophenone → 3-Ethylbenzophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | 3-Ethylbenzophenone | HCID 583730 | — |
Reaction Steps
Friedel-Crafts alkylation is carried out with benzophenone and diethyl sulfate in the presence of aluminum chloride to form 3-ethylbenzophenone. It is then subjected to bromination using N-bromosuccinimide to produce 3-(1-bromoethyl)benzophenone, which is then subjected to alkali hydrolysis to obtain 3-(1-hydroxyethyl)benzophenone. This compound is further reacted with carbon monoxide to obtain ketoprofen (Spanish Patent No. 452,500). ##STR4##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04922052 |
| Source dataset | uspto-grants-1990_05 |
| ORD ID | ord-8ca69273dd56416994935a28a98e1360 |
| Source note | uspto-grants-1990_05 |