Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3,4-Dibromothiophene | HCID 18452 | — |
| Reactant | Stannane, trimethyl(4-methylphenyl)- | HCID 617834 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 19789709 | HCID 19789709 | 45% |
Reaction Steps
Through a solution of p-tolyltrimethyltin (3.17 g, 12.4 mmol) in dry toluene (8 mL) was bubbled N2 for 5 min to degas the solution. To this was added 3,4-dibromothiophene (2.31 g, 9.56 mmol) and a catalytic amount of Pd(PPh3)4 (552 mg, 5 mol %). The reaction mixture was brought to reflux (120° C.) and left overnight. The reaction was cooled to rt and the toluene and replaced by EtOAc. The insoluable salts were removed by filtration through a plug of celite. The product was purified by flash chromatography on a silica column eluting with hexane to afford 1.09 g (45%) of the titled compound as a clear, colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05177074 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-1ea0dd6172b74d4ba645116bbedce795 |
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| Source note | uspto-grants-1993_01 |
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