HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 499975Erstellt: 25. Oktober 2026
Tributyltin Chloride → cis-1-Ethoxy-2-(tri-n-butylstannyl)ethylene
https://huagongshe.com/reaction/499975
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tributyltin Chloride | HCID 15096 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | (1Z)-1-Bromo-2-ethoxyethene | HCID 5386777 | — |
| Edukt | HCID 178418306 | HCID 178418306 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Lösungsmittel | Pentane | HCID 8003 | — |
| Produkt | cis-1-Ethoxy-2-(tri-n-butylstannyl)ethylene | HCID 5706773 | — |
Reaktionsschritte
(Ref. Wollenberg, R. H.; Albizati, K. F.; Peries, R. J. Am. Chem. Soc. 1977, 99, 22, 7365-7367.) To a −78° C. solution of (Z)-2-ethoxy-1-bromoethene (5.0 mL, 46.8 mmol) in diethyl ether (160 mL) was added a 1.7 M solution of tert-butyl lithium in pentane (55 mL), dropwise over 20 min. This pale yellow solution was stirred at −78° C. for 40 min, and then chloro-tri-n-butylstannane (13.3 mL, 49.0 mmol) was added, dropwise over 7 minutes. The resulting reaction mixture was allowed to warm slowly. Once the cooling bath had reached −30° C., saturated aq. NaHCO3 (150 mL) was added, and the cooling bath was removed. This mixture was stirred for 15 minutes, and then the layers were separated. The aq. layer was extracted with diethyl ether (2×50 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated to afford (Z)-2-ethoxy-1-tri-n-butylstannanylethene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07767815B2 |
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| Quelldatensatz | uspto-grants-2010_08 |
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| ORD ID | ord-ea388c30fc5d41d69b8c89fc5b0633a5 |
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| Quellennotiz | uspto-grants-2010_08 |
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