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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1639845Erstellt: 25. Oktober 2026

Water → ethyl(2E)-3-(1,2,3-benzothiadiazol-7-yl)acrylate

https://huagongshe.com/reaction/1639845

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethyl phosphonoacetateHCID 13345—
EduktSodium hydrideHCID 24758—
EduktBenzo[d][1,2,3]thiadiazole-7-carbaldehydeHCID 14835681—
LösungsmittelTetrahydrofuranHCID 8028—
Produktethyl(2E)-3-(1,2,3-benzothiadiazol-7-yl)acrylateHCID 6672064898,2%

Reaktionsschritte

To a suspension of 55% sodium hydride (1.81 g, 41.5 mmol) in tetrahydrofuran (30 mL) was added a solution of ethyl diethylphosphonoacetate (8.31 mL, 41.5 mmol) in tetrahydrofuran (10 mL) at 0° C. and the mixture was stirred for 20 min. To the reaction mixture was added a solution of 1,2,3-benzothiadiazole-7-carbaldehyde (6.20 g, 37.8 mmol) in tetrahydrofuran (60 mL) at 0° C. and the mixture was stirred at room temperature for 4 hr. Water was added and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/1) and recrystallization (ethyl acetate/hexane) to give the title compound (8.70 g, yield 98%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08110585B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-4b0a602c34f14e11b86034dc0869918a
Quellennotizuspto-grants-2012_02