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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 452699Erstellt: 25. Oktober 2026

Carbon Disulfide → HCID 44590954, Verbindung

https://huagongshe.com/reaction/452699

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DisulfideHCID 6348—
EduktPotassium HydroxideHCID 14797—
Edukt3-Fluoro-4-methoxybenzyl chlorideHCID 2060903—
Edukt2,3-Dihydro-1-benzofuran-5-carbohydrazideHCID 18526469—
LösungsmittelEthanolHCID 702—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 44590954HCID 4459095467%

Reaktionsschritte

To a solution of 2,3-dihydro-1-benzofuran-5-carbohydrazide (356 mg, 2.00 mmol) and potassium hydroxide (85%, 198 mg, 3.00 mmol) in ethanol (15 mL) was added carbon disulfide (0.180 mL, 3.00 mmol), and the resulting mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure, a mixture of the obtained residue and N,N-dimethylformamide (10 mL) was tightly sealed in a vial, and the microwave was irradiated at 150° C. for 30 sec. After cooling to room temperature, 3-fluoro-4-methoxybenzyl chloride (698 mg, 4.00 mmol) was added, and the resulting mixture was stirred for 2 hr. The reaction mixture was diluted with ethyl acetate, washed twice with water and once with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was crystallized from hexane/ethyl acetate to give the title compound (478 mg, yield 67%) as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08492378B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-7ecb29a39cb84233a9a132e3035b270c
Quellennotizuspto-grants-2013_07