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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1985018생성일: 2026년 10월 24일

4-Hydroxybenzoic acid hydrazide → 4-Hydroxy-benzoic acid (5-ethyl-thiophen-2-ylmethylene)-hydrazide

https://huagongshe.com/ko/reaction/1985018

반응식

참여 물질

역할이름HCID투입량
반응물4-Hydroxybenzoic acid hydrazideHCID 1742—
반응물5-Ethyl-2-thiophenecarboxaldehydeHCID 169830—
촉매Acetic AcidHCID 176—
용매EthanolHCID 702—
생성물4-Hydroxy-benzoic acid (5-ethyl-thiophen-2-ylmethylene)-hydrazideHCID 359532096.6%

반응 단계

To a solution of 4-hydroxy-benzoic acid hydrazide (0.3 g, 0.002 mol) and 5-ethyl-2-thiophenecarboxaldehyde (0.28 g, 0.002 mol) in abs. EtOH (10 mL), was added 1 drop of acetic acid. The reaction mixture was refluxed for 4 hours. The reaction mixture was cooling to room temperature and concentrated to remove solvent. The resulting residue was solidified by EtOAc to give white solid 0.53 g, in 96% yield, mp: 194.5° C. 1H NMR (CD3OD) δ 8.39 (s, 1H), 7.79 (d, 2H), 7.19 (s, 1H), 6.86 (d, 2H), 6.80 (s, 1H), 2.86 (q, 2H), 1.31 (t, 3H). 13C NMR (CDCl3) δ 166.5, 162.7, 153.1, 144.9, 137.7, 132.3, 130.8, 125.3, 124.8, 116.3, 24.7, 16.2. Anal. Calcd for C14H14N2O2S : C, 61.29; H, 5.14; N, 10.21. Found: C, 61.00; H, 5.18; N, 10.00.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07544838B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-539847714a9f4bb2a1b25d18d7e24a23
출처 메모uspto-grants-2009_06