Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (4-(Diphenylamino)phenyl)(phenyl)methanone | HCID 10545746 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-benzyl-N,N-diphenylaniline | HCID 23399489 | 86% |
Reaction Steps
Lithium aluminum hydride (1.6 g, 43.0 mmol) was dissolved in purified tetrahydrofuran (30 mL) under a nitrogen atmosphere, and the reaction solution was stirred. A solution prepared by dissolving (4-(diphenylamino)phenyl) (phenyl)methanone (5.0 g, 14.3 mmol) in purified tetrahydrofuran (100 mL) was slowly added thereto at 0° C. The reaction mixture solution was stirred at room temperature for 2 hours, and then distilled water (30 mL) was added to the reaction mixture solution, followed by addition of aqueous sodium hydroxide solution (100 mL). The reaction solution was subjected to extraction with dichloromethane, the solvent was removed from the extracted material, and then the residue material was dried in vacuum to thereby obtain a white solid (4.1 g, yield: 86%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476474B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-173202c4f4714e379ea78816da942b1c |
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| Source note | uspto-grants-2013_07 |
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