Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 264823Erstellt: 25. Oktober 2026

Sulfuric Acid → ethyl 2,2-bisfluoromethyl-6-iodo-2H-1-benzopyran-4-carboxylate

https://huagongshe.com/reaction/264823

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktPotassium IodideHCID 4875—
Eduktethyl 6-amino-2,2-bisfluoromethyl-2H-1-benzopyran-4-carboxylateHCID 19037020—
EduktSodium NitriteHCID 23668193—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
Produktethyl 2,2-bisfluoromethyl-6-iodo-2H-1-benzopyran-4-carboxylateHCID 1903701665,9%

Reaktionsschritte

A mixture of 1.09 g of sodium nitrite, 10 ml of methylene chloride and 10 ml of water was added to a mixture of 4.0 g of ethyl 6-amino-2,2-bisfluoromethyl-2H-1-benzopyran-4-carboxylate, 1.66 g of sulfuric acid and 40 ml of water under ice cooling, followed by stirring under ice cooling for 10 minutes. Further, a mixture of 2.85 g of potassium iodide and 5 ml of water was added to the reaction mixture, followed by stirring at room temperature for 1.5 hour. Water was added to the reaction mixture, and the mixture was extracted with methylene chloride. The organic layer was washed with a 20% aqueous solution of sodium sulfite and a brine and then dried over sodium sulfate. The residue obtained by concentration under reduced pressure was subjected to silica gel column chromatography (an eluting solvent, ethyl acetate:hexane=1:1) to obtain 3.67 g of ethyl 2,2-bisfluoromethyl-6-iodo-2H-1-benzopyran-4-carboxylate having a melting point of 89°-90° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646310
Quelldatensatzuspto-grants-1997_07
ORD IDord-396308a5c7c94194a0dbdaf1402b389f
Quellennotizuspto-grants-1997_07