Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475504Generated: October 26, 2026

Acetic Acid → 1-Benzyl-5-oxo-1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/475504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrazine, (phenylmethyl)-, hydrochloride (1:1)HCID 14084—
Reactant(4-Ethoxy-2-oxo-cyclopent-3-enyl)oxo-acetic acid tert-butyl esterHCID 58713641—
SolventEthanolHCID 702—
Product1-Benzyl-5-oxo-1,4,5,6-tetrahydro-cyclopentapyrazole-3-carboxylic acid tert-butyl esterHCID 5871364562.1%

Reaction Steps

To a solution of the intermediate from step A (2.15 g, 8.45 mmol) in ethanol (100 mL) was added benzyl hydrazine hydrochloride (1.8 g, 9.22 mmol) and HOAc (10 mL). The reaction mixture was stirred at room temperature for 16 hours and then refluxed at 70° C. for 30 minutes. The reaction was cooled to room temperature and concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with water, saturated NaHCO3, and brine. The organic layer was dried over anhydrous Na2SO4 filtered and concentrated in vacuo. The residue was purified by flash chromatography (SiO2) using 30% ethyl acetate-hexanes to give the desired product (1.64 g) a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637555B2
Source datasetuspto-grants-2014_01
ORD IDord-c726fce1cffe49cd853f5fc42cabe192
Source noteuspto-grants-2014_01