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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2116663Erstellt: 26. Oktober 2026

Iodoethylene → 1,1,1-Trifluoro-2-(2-mercapto-1,3-thiazol-5-yl)but-3-en-2-ol

https://huagongshe.com/reaction/2116663

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodoethyleneHCID 68976—
EduktHCID 178418306HCID 178418306—
EduktHCID 178519847HCID 178519847—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1,1,1-Trifluoro-2-(2-mercapto-1,3-thiazol-5-yl)but-3-en-2-olHCID 178458803—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of vinyl iodide (1.88 g, 12.2 mmol) in Et2O at −78° C. was added t-butyl lithium (14.3 ml, 1.7 M/pentane, 24.3 mmol). The mixture was stirred at −78° C. for 1 h and warmed up to −30° C. for 5 min. The mixture was cooled back to −78° C. and 2,2,2-trifluoro-1-(2-mercapto-1,3-thiazol-5-yl)ethanone (1.18 g, 5.53 mmol) in Et2O was added. The reaction mixture stirred 30 min at −78° C., brought to 0° C. and partitioned between aqueous NH4Cl and EtOAc. The layers were separated and the aqueous phase was extracted with EtOAc. The combined organic layers were washed with brine and dried over anhydrous Na2SO4. The solvent was evaporated and the residue chromatographed on silica gel (toluene/acetone; 90:10) to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07439260B2
Quelldatensatzuspto-grants-2008_10
ORD IDord-6688bbe9cb174e38b23a8b7707a6b987
Quellennotizuspto-grants-2008_10