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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 512723Erstellt: 26. Oktober 2026

Diisopropylethylamine → Tyclopyrazoflor

https://huagongshe.com/reaction/512723

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktPoly(difluoromethylene), alpha-(2-((2-carboxyethyl)thio)ethyl)-omega-fluoro-HCID 171658—
Edukt3-chloro-N-ethyl-1-(pyridin-3-yl)-1H-pyrazol-amineHCID 118022192—
LösungsmittelEthyl AcetateHCID 8857—
ProduktTyclopyrazoflorHCID 8670062794%

Reaktionsbedingungen

Temperatur27.5 °C

Reaktionsschritte

A solution of 3-((3,3,3-trifluoropropyl)thio)propanoic acid (2.18 g, 10.8 mmol) and 3-chloro-N-ethyl-1-(pyridine-3-yl)-1H-pyrazol-amine (2.00 g, 8.98 mmol) in ethyl acetate (16 mL) was cooled to 5° C. Diisopropylethylamine (5.15 mL, 29.6 mmol) was added dropwise at 0-5° C. over 30 minutes, followed by the addition of 2,4,6-tripropyl-trioxatriphosphinane-2,4,-trioxide (4.00 g, 12.6 mmol) over 30 minutes at 0-5° C. The reaction was allowed to warm to 25-30° C. and stirred for 2 h. Upon reaction completion, the reaction mixture was cooled to 0-5° C. and quenched with water (12 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (30 mL). The combined organic layers were concentrated to afford the desired product as an oil (3.40 g, 94%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09102654B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-15f67a1d8a62450fac2f4ac96c817f78
Quellennotizuspto-grants-2015_08