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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 70902Erstellt: 23. Oktober 2026

Tributylvinyltin → Ethyl 2-vinylthiazole-5-carboxylate

https://huagongshe.com/de/reaction/70902

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTributylvinyltinHCID 81998—
EduktEthyl 2-bromothiazole-5-carboxylateHCID 3614103—
KatalysatorHCID 178418476HCID 178418476—
Lösungsmittel1,4-DioxaneHCID 31275—
ProduktEthyl 2-vinylthiazole-5-carboxylateHCID 5960757189,8%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of tributyl(vinyl)stannane (0.92 mL, 3.14 mmol) and ethyl 2-bromothiazole-5-carboxylate (0.38 mL, 2.54 mmol) in dioxane (33 mL) is added Pd(PPh3)2Cl2 (182 mg, 0.26 mmol) at room temperature. After stirring at 100° C. under nitrogen for 4 hours, the solution is cooled to ambient temperature and then quenched with H2O. The crude is diluted with EtOAc, the organic layer is washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The obtained residue is purified by flash column chromatography on silica gel (eluent: heptane/EtOAc=90:10 to 80:20) to give ethyl 2-vinylthiazole-5-carboxylate (418 mg). HPLC retention time=0.45 minutes (condition B); MS (m+1)=184.1; 1H NMR (400 MHz, CD3OD) δ ppm 1.37 (t, J=7.2 Hz, 3 H) 4.35 (q, J=7.1 Hz, 2 H) 5.71 (d, J=10.9 Hz, 1 H) 6.24 (d, J=17.4 Hz, 1 H) 6.93 (dd, J=17.4, 10.9 Hz, 1 H) 8.29 (s, 1 H)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822534B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-dbd8097989f9421896e1ccd214e01c2b
Quellennotizuspto-grants-2014_09