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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 227821Erstellt: 24. Oktober 2026

(Phenylmethyl)hydrazine → 3,4-Dichloro-6-phenylpyridazine

https://huagongshe.com/de/reaction/227821

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(Phenylmethyl)hydrazineHCID 11157—
Edukt2-Oxo-4-phenylbutyric acidHCID 69732—
EduktSodium MethoxideHCID 10942334—
Edukt3,4-Dichloro-6-phenylpyridazineHCID 13163231—
LösungsmittelMethanolHCID 887—
Produkt3,4-Dichloro-6-phenylpyridazineHCID 13163231—
ProduktHCID 13342056HCID 13342056—
Produkt3-Methoxy-4-chloro-6-phenylpyridazineHCID 66731998—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

3,4-Dichloro-6-phenylpyridazine was synthesized from □-oxobenzenebutanoic acid and 1-(phenylmethyl)hydrazine in 2 steps according to a procedure by Sircar (Sircar, I. J Het. Chem. 1983, 20,1473-1476.) 3,4-Dichloro-6-phenylpyridazine (100 mg, 0.44 mmol) was combined with sodium methoxide (1.1 mL of a 0.50M solution in methanol, 0.55 mmol, 1.25 equiv.) and methanol (296 μl, 1.5M) in a resealable tube and heated to 65° C. for 1 hour. The methanol was evaporated in vacuo, and water was added to the residue. The mixture was extracted with DCM, dried over K2CO3, filtered and concentrated in vacuo, to afford 3,4-dimethoxy-6-phenylpyridazine and 3-methoxy-4-chloro-6-phenylpyridazine, the title compound, as a solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560551B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-667bead50e7a433e8d7e7c138df62023
Quellennotizuspto-grants-2009_07