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HRID 11185作成日:2026年10月27日

3,5-Dichlorobenzoyl chloride → 3,5-dichloro-N'-[4-(octyloxy)benzoyl]benzohydrazide

https://huagongshe.com/reaction/11185

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-Dichlorobenzoyl chlorideHCID 76191—
反応物2-(2,5-Dibromophenyl)-5-[4-(octyloxy)phenyl]-1,3,4-oxadiazoleHCID 21982073—
生成物3,5-dichloro-N'-[4-(octyloxy)benzoyl]benzohydrazideHCID 2198210960%

反応手順

By the general method for the synthesis of 2-(2,5-dibromophenyl)-5-[4-(octyloxy)phenyl]-1,3,4-oxadiazole (1) in Example 3, the reaction of 3,5-dichlorobenzoyl chloride (20.0 g, 0.010 mole) with 4-octoxybenzoyl hydrazide (25.24 g, 0.010 mole) gave the intermediate 3,5-dichloro-N′-[4-(octyloxy)benzoyl]benzohydrazide (25 g, 60% yield). Cyclocondensation of the intermediate 3,5-dichloro-N′-[4-(octyloxy)benzoyl]-benzohydrazide (16.0 g) with POCl3 (83 mL) gave the required 2-(3,5-dichlorophenyl)-5-[4-(octyloxy)phenyl]-1,3,4-oxadiazole (4) (11.16 g, 73% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07094902B2
出典データセットuspto-grants-2006_08
ORD IDord-7768084908b14dee8441d1827dd3fcea
出典メモuspto-grants-2006_08