HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602056Generated: October 31, 2026
Tributylvinyltin → HCID 57470605, compound
https://huagongshe.com/reaction/602056
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylvinyltin | HCID 81998 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 68790034 | HCID 68790034 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 57470605 | HCID 57470605 | 60% |
Reaction Steps
To a solution of ethyl 2-{3,4-difluoro-5-[(trifluoroacetyl)oxy]phenyl}-2-methylpropanoate (113 mg, 0.332 mmol) in DMF (6 mL, deoxygenated with N2) under N2 was added (t-Bu3P)2Pd (25 mg, 0.05 mmol), lithium chloride (42 mg, 0.996 mmol), and vinyl(tributyl)tin (0.11 mL, 0.365 mmol). The reaction was stirred at room temperature for 22 hours. To the reaction mixture was added ethyl acetate and 20% KF (aq.) and the reaction stirred for an additional 2 h. The suspension was filtered through and rinsed with ethyl acetate. The organic layer was washed with 20% KF (aq.). The combined aqueous layers were washed with ethyl acetate. The combined organic layers were then washed with H2O and brine, dried, and purified by Biotage purification system using (0-80% DCM:hexane) yielded the desired product (50 mg, 60%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07902394B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-18a7652a259d4ad58afa2c045eea2431 |
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| Source note | uspto-grants-2011_03 |
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