Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylstannane | HCID 5948 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 20060989 | HCID 20060989 | — |
| Product | HCID 20061023 | HCID 20061023 | — |
Reaction Steps
A solution of the product from (b) (1.03 g, 3 mmol) and tetrakis (triphenylphosphine)palladium (0.3 g) in THF (70 ml) was installed under an atmosphere of carbon monoxide and heated to 50° C. Tributyltin hydride (0.96 g, 3.3 mmol) in THF (40 ml) was instilled by motor-driven syringe over 4.5 hours. After an additional 0.5 hours the mixture was stirred with 100 ml of 10% potassium fluoride solution for 15 minutes, then extracted twice with dichloromethane. The organic layers were dried over magnesium sulphate and evaporated to an orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05008263 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-8515b0802c154cb3bfff6ca4b2bbdeb1 |
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| Source note | uspto-grants-1991_04 |
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