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HRID 499975Erstellt: 25. Oktober 2026

Tributyltin Chloride → cis-1-Ethoxy-2-(tri-n-butylstannyl)ethylene

https://huagongshe.com/reaction/499975

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributyltin ChlorideHCID 15096—
EduktSodium BicarbonateHCID 516892—
Edukt(1Z)-1-Bromo-2-ethoxyetheneHCID 5386777—
EduktHCID 178418306HCID 178418306—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelPentaneHCID 8003—
Produktcis-1-Ethoxy-2-(tri-n-butylstannyl)ethyleneHCID 5706773—

Reaktionsbedingungen

Temperatur-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07767815B2
Quelldatensatzuspto-grants-2010_08
ORD IDord-ea388c30fc5d41d69b8c89fc5b0633a5
Quellennotizuspto-grants-2010_08