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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384309Generated: October 30, 2026

Methanol → 2-(2,3-Dihydro-benzofuran-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-one

https://huagongshe.com/reaction/384309

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantEthyl AcetoacetateHCID 8868—
ReactantAmmonium AcetateHCID 517165—
ReactantBis(2,2,2-trichloroethyl) 1-(2,3-dihydrobenzofuran-5-yl)hydrazine-1,2-dicarboxylateHCID 10505571—
CatalystZincHCID 23994—
SolventEthanolHCID 702—
Product2-(2,3-Dihydro-benzofuran-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-oneHCID 5748378156.5%

Reaction Steps

Bis(2,2,2-trichloroethyl) 1-(2,3-dihydrobenzofuran-5-yl)hydrazine-1,2-dicarboxylate 7b (2.9 g, 5.8 mmol) was dissolved in 50 mL of ethanol and 5 mL of methanol followed by addition of zinc powder (10.8 g, 166 mmol) and aqueous ammonium acetate (15 mL, 1 mol/L) and the mixture was reacted at room temperature for 1 hour. Then ethyl acetoacetate (0.75 mL, 5.9 mmol) was added dropwise. The reaction mixture was heated to reflux for 2 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The reaction was cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography to obtain the title compound 2-(2,3-dihydro-benzofuran-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-one 7c (706 mg, yield 56.5%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-0f8fdde974ed49929712f5cbf70bb9fc
Source noteuspto-grants-2013_02