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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 366297Erstellt: 26. Oktober 2026

(E)-1,3-Dichloropropene → (E)-2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methyl-6-(3-chloroprop-2-enyloxy)pyridine

https://huagongshe.com/reaction/366297

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(E)-1,3-DichloropropeneHCID 24726—
EduktSodium hydrideHCID 24758—
EduktHCID 178429419HCID 178429419—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelEthyl acetate pentaneHCID 22335286—
Produkt(E)-2-(1-Methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methyl-6-(3-chloroprop-2-enyloxy)pyridineHCID 1547717452,3%

Reaktionsschritte

A mixture of 6-hydroxy-2-(1-methyl-3-trifluoromethylpyrazol-5-yloxy)-4-methylpyridine (0.9 g, 3.3 mmol) and NaH (60 % in oil, 0.16 g, 4 mmol) in acetonitrile (20 ml) and DMF (1 ml) is stirred for 10 min at ambient temperature and (E)-1,3-dichloropropene (0.4 g, 3.6 mmol) is added. After stirring for 60 h at ambient temperature, the remaining NaH is deactivated and the resulting mixture is diluted with pentane/ethyl acetate (by volume ration 1/1) and filtered through a bed of silica gel. The filtrate is washed with water. The organic layer is dried with anhydrous magnesium sulfate, filtered and evaporated in vacuo. Purification by flash chromatography (silica gel: pentane/ethyl acetate 9/1 v/v) yields the title compound (0.6 g, 52 % yield) as an colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06130188
Quelldatensatzuspto-grants-2000_10
ORD IDord-34dd5c0c7f8a40b59706a99c17232257
Quellennotizuspto-grants-2000_10