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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 854949Erstellt: 24. Oktober 2026

Potassium Carbonate → ethyl 6-chloro-5,7-dimethyl-2-(trifluoromethyl)-2H-chromene-3-carboxylate

https://huagongshe.com/de/reaction/854949

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt3-Chloro-6-hydroxy-2,4-dimethylbenzaldehydeHCID 3335082—
EduktEthyl (2E)-4,4,4-trifluoro-2-butenoateHCID 5371261—
LösungsmittelDimethylformamideHCID 6228—
Produktethyl 6-chloro-5,7-dimethyl-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 69339659110,2%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

To a solution of 3-chloro-6-hydroxy-2,4-dimethylbenzaldehyde (6.9 g, 37.4 mmol) in 80 mL of DMF was added dried finely powdered K2CO3 (11.36 g, 82.2 mmol). With mechanical stirring, the reaction was heated to 65° C. To the suspension was added dropwise ethyl trifluorocrotonate (7.54 g, 44.9 mmol). The stirring reaction was heated at 90° C. for 1.5 h. K2CO3 was filtered from the cooled reaction. From the reaction under vacuum, DMF was removed. The resulting residue was dissolved in 400 mL EtOAc. The organic solution was washed with 100 mL 1 M KHSO4, 70 mL of satd. KHCO3, 100 mL brine, followed by drying over MgSO4, and concentrating under vacuum. The crude desired product (13.8 g) of was isolated. After employing flash chromatography conditions, pure compound (9.8 g, 78%) of was isolated and its structure confirmed by NMR and LC-MS.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07259266B2
Quelldatensatzuspto-grants-2007_08
ORD IDord-42540ae1ea6d43768d62b998090f1aae
Quellennotizuspto-grants-2007_08