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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 458492생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/458492

반응식

참여 물질

역할이름HCID투입량
반응물4-Octoxybenzoyl hydrazineHCID 4281533—
반응물3,5-Dibromobenzoyl chlorideHCID 13450526—
반응물2-(2,5-Dibromophenyl)-5-[4-(octyloxy)phenyl]-1,3,4-oxadiazoleHCID 21982073—
생성물3,5-dibromo-N'-[4-(octyloxy)benzoyl]benzohydrazideHCID 2198208136%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07192657B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-def7b1a82ede453eb42287d0f43d1b25
출처 메모uspto-grants-2007_03