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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1797833Erstellt: 27. Oktober 2026

Benzoyl chloride → 1-Benzoyl-2-(4-iodobenzoyl)hydrazine

https://huagongshe.com/reaction/1797833

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktN-methyl-2-pyrrolidoneHCID 13387—
Edukt4-IodobenzenecarbohydrazideHCID 306104—
LösungsmittelWaterHCID 962—
Produkt1-Benzoyl-2-(4-iodobenzoyl)hydrazineHCID 480893797%

Reaktionsschritte

Into a 300 mL three-neck flask was put 15 g (57 mmol) of 4-iodobenzoylhydrazine, 15 mL of N-methyl-2-pyrrolidone (NMP) was added thereto, and the mixture was stirred for 10 minutes at a room temperature. After the stirring, 50 mL of a mixed solution of 5 mL of N-methyl-2-pyrrolidone and 7.9 mL (69 mmol) of benzoyl chloride was dripped into the solution through a dropping funnel, and the solution was stirred at a room temperature for 18 hours. After the stirring, water was added into the solution, and a solid was precipitated. The precipitated solid was collected by suction filtration. The collected solid was added into about 500 mL of a saturated aqueous solution of sodium hydrogen carbonate, stirred, and washed. After the washing, the mixture was subjected to suction filtration to obtain a solid. The obtained solid was added into about 500 mL of water, stirred, and washed. After the washing, the mixture was subjected to suction filtration to obtain a solid. The obtained solid was washed with methanol to give 20 g of a powdery white solid in a yield of 97%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08343639B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-f0ece7b2d05d4470964092363d930256
Quellennotizuspto-grants-2013_01