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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 388271Erstellt: 24. Oktober 2026

Methyl phenylacetate → Benzeneacetic acid, hydrazide

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl phenylacetateHCID 7559—
EduktHydrazine hydrate (1:1)HCID 24654—
Edukt4-Fluoromandelic acidHCID 98068—
LösungsmittelEthanolHCID 702—
ProduktBenzeneacetic acid, hydrazideHCID 70301—

Reaktionsschritte

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)).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08377930B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-dc6962bb739740efbb0c03a2685632cd
Quellennotizuspto-grants-2013_02