Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | 5-Bromo-2-chloroanisole | HCID 2769567 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Benzophenone | HCID 3102 | — |
Reaction Steps
After 8.7 g (357.06 mmol) of Mg and a small amount of iodine were dissolved in 200 ml of THF, 71.9 g (324.6 mmol) of 5-bromo-2-chloroanisole 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. After that, the prepared Grignard reagent was added dropwise to 50.2 g (357.06 mmol) of benzoyl chloride 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 (32) as 32.0 g (129.8 mmol, yield of 40%) of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916071B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-40e6317a9e2343e7ae72c881dcaf7dc6 |
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| Source note | uspto-grants-2014_12 |
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