HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 887136Erstellt: 25. Oktober 2026
Tributylstannane → Benzyl 2-(tributylstannyl)acrylate
https://huagongshe.com/reaction/887136
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tributylstannane | HCID 5948 | — |
| Edukt | Benzyl propiolate | HCID 543064 | — |
| Katalysator | HCID 178418397 | HCID 178418397 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | Benzyl 2-(tributylstannyl)acrylate | HCID 66838741 | 73% |
Reaktionsschritte
To a solution of 6.42 g (40.1 mmol) of benzyl propiolate from step A above in 25 ml of anhydrous THF was added 0.93 g (0.80 mmol) of tetrakis(triphenylphosphine)palladium(0) followed by a solution of 12.6 g (42.1 mmol) of tributyltin hydride in 25 mL of anhydrous THF over 15 min. After stirring at room temperature overnight the solvent was removed under reduced pressure. The residue was filtered through a pad of Celite® which was then washed with hexanes. The filtrate was concentrated in vacuo and the crude product was purified by silica gel chromatography eluting with a 0-15% ethyl acetate in hexane gradient to afford the title compound as a colorless oil (13 g, 73%). 1H NMR (CDCl3, 500 MHz) δ 7.39 (m, 5H), 6.99 (d, J=2.7 Hz, 1H), 5.98 (d, J=2.7 Hz, 1H), 5.20 (s, 2H), 1.47 (m, 6H), 1.30 (m, 6H), 0.96 (m, 6H), 0.89 (t, J=7.4 Hz, 9H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08247415B2 |
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| Quelldatensatz | uspto-grants-2012_08 |
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| ORD ID | ord-9c278a474edc4e2da10fc3245a175092 |
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| Quellennotiz | uspto-grants-2012_08 |
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