Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1488382Erstellt: 27. Oktober 2026

Hydrochloric Acid → 4-[5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrophenoxy]-3-oxo-2-(2,4-dichlorophenyl)-pentanenitrile

https://huagongshe.com/reaction/1488382

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt2,4-DichlorophenylacetonitrileHCID 80566—
Edukt2-[2-Nitro-5-(2-chloro-4-trifluoromethylphenoxy)phenoxy]propionyl ChlorideHCID 13100684—
EduktHCID 178418244HCID 178418244—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-[5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrophenoxy]-3-oxo-2-(2,4-dichlorophenyl)-pentanenitrileHCID 22904777—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A solution of 0.93 g of 2,4-dichlorophenylacetonitrile in 30 ml of anhydrous tetrahydrofuran (hereinafter abbreviated as "THF") was cooled to -78° C. To this solution was added 3.5 ml of a 1.6Mn BuLi-hexane solution. Then, a THF solution of 2.12 g of 2-[5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrophenoxy]propionic acid chloride was added thereto dropwise. The mixed solution was stirred for 30 minutes, then acidified with a 10% hydrochloric acid aqueous solution, and extracted with ethyl acetate. The ethyl acetate layer was dried over anhydrous magnesium sulfate, filtered and concentrated with a rotary evaporator.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05674811
Quelldatensatzuspto-grants-1997_10
ORD IDord-67b52b8b130a4511a6c1240f92044ef8
Quellennotizuspto-grants-1997_10