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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 917356Erstellt: 25. Oktober 2026

Dimethylformamide → 6,6-Difluoro-5-methyl-5-hexenyl 4-methyl-2-phenylthiazole-5-carboxylate

https://huagongshe.com/reaction/917356

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktSodium BicarbonateHCID 516892—
Edukt4-Methyl-2-phenyl-thiazole-5-carboxylic acidHCID 720957—
Edukt6,6-Difluoro-5-methyl-5-hexenyl methanesulfonateHCID 23020371—
LösungsmittelWaterHCID 962—
Produkt6,6-Difluoro-5-methyl-5-hexenyl 4-methyl-2-phenylthiazole-5-carboxylateHCID 2302018874%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To 10 ml of N,N-dimethylformamide were dissolved 0.50 g (2.2 mmol) of 6,6-difluoro-5-methyl-5-hexenyl methanesulfonate and 0.53 g (2.4 mmol) of 4-methyl-2-phenylthiazole-5-carboxylic acid, followed by the addition of 0.37 g (4.4 mmol) of sodium hydrogencarbonate and stirring at 100° C. for 6 hours. The reaction liquid was then poured in water and extracted with ethyl acetate. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentration under reduced pressure. The residue was purified with silica gel column chromatography (ethyl acetate:hexane=1:19) to obtain 0.57 g (yield: 74%) of 6,6-difluoro-5-methyl-5-hexenyl 4-methyl-2-phenylthiazole-5-carboxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07273878B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-ed3a289d1c7047d889f544ad0741d157
Quellennotizuspto-grants-2007_09