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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 388271생성일: 2026년 10월 24일

Methyl phenylacetate → Benzeneacetic acid, hydrazide

https://huagongshe.com/ko/reaction/388271

반응식

참여 물질

역할이름HCID투입량
반응물Methyl phenylacetateHCID 7559—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물4-Fluoromandelic acidHCID 98068—
용매EthanolHCID 702—
생성물Benzeneacetic acid, hydrazideHCID 70301—

반응 단계

The following representative compounds in Table 1 were synthesized according to (i) the foregoing procedures by selecting appropriate starting materials (for example, 4-fluoro mandelic acid derivatives (e.g., examples 12-1 and 12-3) were synthesized using commercially available 4-fluoromandelic acid) and (ii) known organic synthesis techniques (for example, treatment of commercially available α-phenylacetic acid methyl ester with hydrazine hydrate in ethanol under with heating provides phenyl-acetic acid hydrazide (see, e.g., Pandeye, S, N.; Manjula, H.; Stables, J. P.; Pharmazie; 2001, 56, 121-124) and treatment of phenyl acetic acid hydrazide with a substituted benzaldehyde in ethanol with heating and in the presence of catalytic acetic acid provides the corresponding substituted phenyl-acetic acid benzylidenehydrazide (see, e.g., Stephanidou-Stephanatou, J.; Lefkopoulou, S; Journal of Heterocyclic Chemistry; 1982; 19; 705-711.0)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08377930B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-dc6962bb739740efbb0c03a2685632cd
출처 메모uspto-grants-2013_02