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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 458492Erstellt: 24. Oktober 2026

4-Octoxybenzoyl hydrazine → 3,5-dibromo-N'-[4-(octyloxy)benzoyl]benzohydrazide

https://huagongshe.com/de/reaction/458492

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Octoxybenzoyl hydrazineHCID 4281533—
Edukt3,5-Dibromobenzoyl chlorideHCID 13450526—
Edukt2-(2,5-Dibromophenyl)-5-[4-(octyloxy)phenyl]-1,3,4-oxadiazoleHCID 21982073—
Produkt3,5-dibromo-N'-[4-(octyloxy)benzoyl]benzohydrazideHCID 2198208136%

Reaktionsschritte

By the general method for the synthesis of 2-(2,5-dibromophenyl)-5-[4-(octyloxy)phenyl]-1,3,4-oxadiazole in Example 1, the reaction of 3,5-dibromobenzoyl chloride (20.13 g, 0.06747 mole) with 4-octyloxybenzoic acid hydrazide (17 g, 0.06747 mole) gave the intermediate 3,5-dibromo-N′-[4-(octyloxy)benzoyl]benzohydrazide (12.87 g, 36% yield). Cyclocondensation of the intermediate 3,5-dibromo-N′-[4-(octyloxy)benzoyl]-benzohydrazide (12.17 g) with POCl3 (63 mL) gave the required 2-(3,5-dibromophenyl)-5-[4-(octyloxy)phenyl]-1,3,4-oxadiazole (6.12 g, 52% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07192657B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-def7b1a82ede453eb42287d0f43d1b25
Quellennotizuspto-grants-2007_03