Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | Tetraethoxysilane | HCID 6517 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Bromo-2,6-diisopropylaniline | HCID 11780114 | — |
| Product | HCID 86041032 | HCID 86041032 | 77% |
Reaction Steps
40.7 g (0.195 mol) of tetraethoxysilane and 0.5 mL of sulfuric acid were added to a flask equipped with a distiller, containing 43.9 g (0.169 mol) of 4-bromo-2,6-diisopropylaniline and 24.8 g (0.130 mol) of benzophenone under a nitrogen atmosphere. The mixture was reacted by heating at 160° C. for 2 days while removing formed ethanol using the distiller. After the reaction, the resultant product was cooled to room temperature. Then, 200 mL of 1.0 M aqueous solution of potassium hydroxide was added to the resultant product and stirred for 10 minutes to obtain yellow precipitates. The obtained precipitates were filtered off and dissolved in 300 mL of ethyl acetate, and then dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure to obtain a yellow solid. Then, the yellow solid was recrystallized in hexane at −20° C. to obtain 42 g of N-diphenylmethylene-2,6-diisopropyl-4-bromoaniline compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07244805B2 |
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| Source dataset | uspto-grants-2007_07 |
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| ORD ID | ord-776327b8ccd34d389d74d57c5e9938ab |
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| Source note | uspto-grants-2007_07 |
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