Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Butylaniline | HCID 7694 | — |
| Reactant | Trans-4,4'-dibromostilbene | HCID 7020566 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 68616059 | HCID 68616059 | — |
Reaction Steps
To a solution of tris(di-benzylideneacetone)dipalladium (Pd2(dba)3) (0.335 g, 0.365 mmol) and bis-(diphenylphosphino)ferrocene (DPPF) (0.294 g, 0.530 mmol) in dry toluene (20 ml) under nitrogen atmosphere was added trans-4,4′-dibromostilbene (10) (2.0 g, 5.91 mmol) at room temperature, and the resultant mixture was stirred for 10 min, sodium tert-butoxide (2.6 g) and 4-n-butyl aniline (1.77 g, 11.83 mmol) were added to this solution and stirred at 90° C. overnight. The solid was collected, washed three times with methanol and ether, and isolated in 68.8% (1.93 g) yield as an NAM-pure product. 1H NMR (CDCl3, 500 MHz) δ ppm: 7.38 (d, J=8.0 Hz, 4H), 7.10 (d, J=8.5 Hz, 4H), 7.03 (d, J=8.0 Hz, 4H), 7.0 (d, J=8.5 Hz, 4H), 6.91 (s, 2H, ═CH), 5.77 (s, 2H, NH), 2.56 (t, J=7.7 Hz, CH2, 4H), 1.59 (m, CH2, 4H), 1.37 (m, CH2, 4H), 0.94 (t, J=7.5Hz, CH3, 6H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07459106B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-806025c519304284a704b55dca7b89bd |
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| Source note | uspto-grants-2008_12 |
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