Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 3-Bromo-N,N-diphenylaniline | HCID 16217851 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67979279 | HCID 67979279 | 88% |
Reaction Steps
First, 0.45 g of magnesium and 5 ml of THF were suspended, and a tiny amount of 1,2-dibromoethane was added to the obtained suspension. A mixed solution of 3.0 g of 3-bromo-N,N-diphenylaniline and 30 mL of THF was dripped to this suspension, and the mixture was stirred while being heated under reflux for 1.5 hours to cause a reaction. After the reaction, the solution which was naturally cooled to room temperature was cooled to −78° C., and 1.95 g of trimethyl borate was added thereto. The mixture was stirred while the temperature was increased to room temperature to cause a reaction. After the reaction, the solution was concentrated, and 4.8 mL of ethylene glycol and 30 mL of toluene were added to the obtained residue. The mixture was stirred while being heated under reflux for 12 hours to cause a reaction. After the reaction, the solution was filtered and the obtained filtrate was concentrated, so that a while solid was obtained (88% yield). The synthesis scheme of Step 1 is shown by (a-1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735581B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-9501879bb27d434cac6e65d657ec377d |
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| Source note | uspto-grants-2014_05 |
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