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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 339449Erstellt: 24. Oktober 2026

Benzaldehyde → Benzylidene-hydrazine

https://huagongshe.com/de/reaction/339449

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktMethanolHCID 887—
EduktHydrazine hydrate (1:1)HCID 24654—
EduktBarium Oxide Nanoparticle DispersionHCID 9855530—
LösungsmittelDiethyl EtherHCID 3283—
ProduktBenzylidene-hydrazineHCID 957427,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A 1 L flask equipped with a mechanical stirrer, thermometer, and addition funnel was charged with 250 mL of methanol and cooled to 0° C. Barium oxide (9.8 g, 64 mmol) was added portion-wise with exotherm. The reaction was cooled to 0° C., and hydrazine monohydrate (64.1 g, 1.28 mol) was slowly added. The reaction mixture was stirred for 10 minutes, after which time benzaldehyde (135.8 g, 1.28 mol) was added drop-wise over a 30 minute period. The reaction was then stirred for 1 hour, while maintaining a temperature below 8 (C. 1H NMR indicated the absence of ketone and a complete reaction. Ether (200 mL) was added, and the BaO was filtered through a bed of silica gel. The resultant clear filtrate was liberated of methanol on a rotary evaporator at or below room temperature. A large mass of bright yellow solid azine (1H-NMR (300 MHz, CDCl3) δ (ppm): 8.67 (s, 2H), 7.85 (m, 4H), 7.47 (m, 6H)), was removed by filtration, and the filtrate was distilled to provide ca. 12 g of distillate benzylidene-hydrazine. The material was stored under refrigeration. 1H-NMR (300 MHz, CDCl3) δ (ppm): 7.74 (s, 1H), 7.53 (m, 2H), 7.35 (m, 3H), 5.5 (br, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08895306B2
Quelldatensatzuspto-grants-2014_11
ORD IDord-afcdc90991a942b0ba52dee8c77f2278
Quellennotizuspto-grants-2014_11