Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 4-Bromo-1-chloro-2-ethoxybenzene | HCID 50998187 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzophenone | HCID 3102 | — |
Reaction Steps
8.7 g (357.06 mmol) of Mg and a small amount of iodine were dissolved in 200 ml of THF, and 84.6 g (324.6 mmol) of 1-bromo-4-chloro-3-ethoxybenzene dissolved in 500 ml of THF was added dropwise to the resulting solution. After addition, the resulting mixture was refluxed for 3 hours to prepare a Grignard reagent which was then cooled to room temperature. Thereafter, a Grignard reagent containing 50.2 g (357.06 mmol) of benzoyl chloride was added dropwise to the obtained product and stirred for 5 hours. After a reaction, the reaction solution was washed with water, the solvent was removed, and the obtained product was purified by column chromatography to obtain a benzophenone derivative represented by the following formula (42) as 29.6 g (113.6 mmol, yield of 35%) of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08916071B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-528072fb6fdb4f9b97e8e7768e3b63ef |
|---|
| Source note | uspto-grants-2014_12 |
|---|