Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | p-Xylyl bromide | HCID 7721 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 59235714 | HCID 59235714 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 59235715 | HCID 59235715 | 175.3% |
Reaction Steps
4-(4′-Diphenylaminobiphenyl-4-yl)pyrimidine-2-amine (100 mg, 0.24 mmol) and sodium hydroxide (38 mg, 0.96 mmol) were added in dimethylsulfoxide (1 mL), and stirred at 100° C. for 30 minutes. This solution was added with a solution of 4-methylbenzyl bromide (71.6 μL, 0.53 mmol) in dimethylsulfoxide (1 mL) at 100° C. for 30 minutes, and stirred for 5 hours. This solution was cooled and added with water (100 mL) and a saturated saline solution, and allowed to stand for 24 hours. The precipitated crystalline material was purified by column chromatogram (silica gel, hexane:EtOAc=8:1) to obtain the title compound (131 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08124762B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-e458627118b243768964723c0398911f |
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| Source note | uspto-grants-2012_02 |
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