Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 917352Erstellt: 24. Oktober 2026

Dimethylformamide → 6,6-Difluoro-5-methyl-5-hexenyl benzo[b]thiophene-2-carboxylate

https://huagongshe.com/de/reaction/917352

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktBenzo(b)thiophene-2-carboxylic acidHCID 95864—
EduktSodium BicarbonateHCID 516892—
Edukt6,6-Difluoro-5-methyl-5-hexenyl methanesulfonateHCID 23020371—
LösungsmittelWaterHCID 962—
Produkt6,6-Difluoro-5-methyl-5-hexenyl benzo[b]thiophene-2-carboxylateHCID 6918169081%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To 40 ml of N,N-dimethylformamide were dissolved 5.00 g (22 mmol) of 6,6-difluoro-5-methyl-5-hexenyl methanesulfonate and 4.30 g (24 mmol) of benzo[b]thiophene-2-carboxylicacid, followed by the addition of 6.00 g (71 mmol) of sodium hydrogencarbonate and stirring at 100° C. for 3 hours. The reaction liquid was then poured in water and extracted with diethyl ether. The organic layer was washed with water and a saturated saline solution in this order, followed by drying over anhydrous magnesium sulfate and concentration under reduced pressure. The residue was purified with silica gel column chromatography (diisopropyl ether:hexane=1:7) to obtain 5.50 g (yield: 81%) of 6,6-difluoro-5-methyl-5-hexenyl benzo[b]thiophene-2-carboxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07273878B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-9db6e71ddd914462931406307e242912
Quellennotizuspto-grants-2007_09