HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388271Generated: October 26, 2026
Methyl phenylacetate → Benzeneacetic acid, hydrazide
https://huagongshe.com/reaction/388271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl phenylacetate | HCID 7559 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-Fluoromandelic acid | HCID 98068 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Benzeneacetic acid, hydrazide | HCID 70301 | — |
Reaction Steps
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)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377930B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-dc6962bb739740efbb0c03a2685632cd |
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| Source note | uspto-grants-2013_02 |
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