Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Benzo(b)thiophene, 3-bromo- | HCID 123250 | — |
| Reactant | HCID 14478582 | HCID 14478582 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15171918 | HCID 15171918 | — |
Reaction Steps
A mixture of 0.544 g of rac-6-acetyloxy-2-ethynyl3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran, 0.64 g of 3-bromobenzothiophene, 90 mg of triphenylphosphine, 20 mg of cuprous iodide, 2 ml of triethylamine and 40 ml of dimethylformamide was stirred and degased by a stream of argon for minutes. Palladium acetate, 30 mg, was then added and the mixture was heated at 95° C. for 5 hours. The reaction mixture was partitioned between saturated sodium bicarbonate solution and toluene. The organic phase was washed with water, dried and evaporated. The residue was chromatographed over 50 g of silica gel using toluene for elution. The combined clean fractions were crystallized from hexane to give the title compound with m.p. 96°-99°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05132310 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-25843b7d606b4615986c601f481d91a3 |
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| Source note | uspto-grants-1992_07 |
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