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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 334511Erstellt: 25. Oktober 2026

Chloroacetyl chloride → 4-chloro-N'-(2-chloroacetyl)benzohydrazide

https://huagongshe.com/reaction/334511

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetyl chlorideHCID 6577—
Edukt4-ChlorobenzohydrazideHCID 10816—
EduktPotassium CarbonateHCID 11430—
LösungsmittelAcetonitrileHCID 6342—
Produkt4-chloro-N'-(2-chloroacetyl)benzohydrazideHCID 52129282,9%

Reaktionsschritte

To a mixture of 4-chlorobenzohydrazide 5 (1 g, 5.86 mmol) and K2CO3 (0.97 g, 7.03 mmol) in acetonitrile (30 mL) was added 2-chloroacetyl chloride (0.68 g, 6.08 mmol) dropwise at ambient temperature. The resulting mixture was stirred at ambient temperature for 16 hours. The solid was collected, washed with H2O and ether, and dried to afford 4-chloro-N′-(2-chloroacetyl)benzohydrazide 6 (1.2 g, 82%) which was used for the next step without further purification. A mixture of 4-chloro-N′-(2-chloroacetyl)benzohydrazide 6 (0.6 g, 2.43 mmol) and phosphorous oxychloride (0.37 g, 2.43 mmol) in acetonitrile (20 mL) was stirred under reflux for 16 hours and concentrated. The residue was subjected to flush column chromatography eluting with 10-25% acetone/hexanes to give compound 7 (0.45 g). Yield: 82%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08883827B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-cd1081c5ecb94ff59ed793d11615e971
Quellennotizuspto-grants-2014_11