HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090193Generated: October 31, 2026
Tri(butyl)vinylstannane → HCID 54049649, compound
https://huagongshe.com/reaction/2090193
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tri(butyl)vinylstannane | HCID 21115800 | — |
| Reactant | 5-Cyano-2-formylphenyl trifluoromethanesulfonate | HCID 59349638 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Product | HCID 54049649 | HCID 54049649 | — |
Reaction Steps
125 mg (0.18 mmol) of bis(triphenylphosphine)palladium(II) chloride are added to a solution of 1 g (3.58 mmol) of 5-cyano-2-formylphenyl trifluoromethanesulfonate and 1.15 ml (3.94 mmol) of tri-n-butylvinylstannane in 6 ml of anhydrous and degassed DMF under an argon atmosphere. The reaction mixture is then stirred at 80° C. for 90 min. Subsequently, 100 ml of 10% strength potassium fluoride solution are added, and the mixture is stirred at RT for 1 h. The suspension is extracted three times with 20 ml of ethyl acetate each time, and the combined organic phases are washed successively with saturated sodium bicarbonate solution and saturated sodium chloride solution. The organic solution is dried over magnesium sulfate and concentrated. The residue (0.6 g) is employed without further purification in the next stage.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08436180B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-1073eeaa064745a0abe2763721e18aac |
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| Source note | uspto-grants-2013_05 |
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