Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Triphenylamine | HCID 11775 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Bromotriphenylamine | HCID 642838 | 67.9% |
Reaction Steps
First, 25 g (100 mmol) of triphenylamine, 18 g (100 mmol) of N-bromosuccinimide, and 400 mL of ethyl acetate were put in a 1000-mL Erlenmeyer flask, and the mixture was stirred at room temperature in the air for 18 hours. After the reaction was terminated, the mixture was washed with a saturated sodium carbonate aqueous solution twice to obtain an organic layer and a water layer. Then, the water layer was extracted twice with ethyl acetate, and the extract was combined with the organic layer and washed with a saturated saline solution. The solution was dried with magnesium sulfate and filtered naturally, and the filtrate was concentrated. An obtained colorless solid was recrystallized with ethyl acetate-hexane; thus, 22 g of a colorless powdered solid of 4-bromotriphenylamine was obtained (yield: 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389735B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-983de6e5849e49c6a9bbe6d491e4a43e |
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| Source note | uspto-grants-2013_03 |
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