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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82310Generated: October 30, 2026

Water → HCID 178434613, compound

https://huagongshe.com/reaction/82310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178483593HCID 178483593—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178434613HCID 17843461389%

Reaction Steps

To a solution of benzyl 3-(methylamino)-2-(trifluoroacetyl)but-2-enoate (90 g, 300 mmol) in a mixture of THF (900 mL) and acetic acid (100 mL) was added hydrazine monohydrate (14.6 mL, 300 mmol) over a 5 min period. The reaction mixture was heated to reflux for 3 hours, allowed to cool to room temperature and the solvents were evaporated in vacuo to afford a bright yellow mass. The mass was dissolved in EtOAc (1 L) and water (1 L) with gentle heating, allowed to cool to room temperature and the aqueous layer was neutralized to pH 7-8 with NaHCO3. This mixture was transferred to a 3-L separating funnel, the layers were mixed vigorously, separated and the organic layer was washed with water (3×500 mL) dried (MgSO4), filtered and evaporated in vacuo to give benzyl 3-methyl-5-(trifluoromethyl)-1H-pyrazole-4-carboxylate as an off-white solid in 89% yield 74 g that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846698B2
Source datasetuspto-grants-2014_09
ORD IDord-b545c12b023d4278a04a10a304bc18ee
Source noteuspto-grants-2014_09