Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylamine | HCID 11775 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-Bromotriphenylamine | HCID 642838 | 67.9% |
Reaction Steps
25 g (100 mmol) of triphenylamine, 18 g (100 mmol) of N-bromosuccinimide, and 400 mL of ethyl acetate were put into a 1000 mL Erlenmeyer flask, and were stirred for approximately 12 hours at the room temperature in the air to be reacted. After the reaction was completed, the reaction solution was washed twice with a saturated sodium carbonate solution to separate an aqueous layer and an organic layer. Then, the aqueous 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 then filtration was performed. The filtrate was concentrated, and an obtained solid of 4-bromotriphenylamine was re-crystallized with ethyl acetate and hexane, whereby 22 g of a white powder solid was obtained in the yield of 66% (Synthesis Scheme (i-1)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09324951B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-eeb0b9fb3fb3456684bfd4bc68ed4b3f |
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| Source note | uspto-grants-2016_04 |
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