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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295262Generated: October 30, 2026

ethyl (E)-3-(3-benzyloxy-1-phenyl-1H-pyrazol-4-yl)propenoate → ethyl 3-(3-benzyloxy-1-phenyl-1H-pyrazol-4-yl)propionate

https://huagongshe.com/reaction/1295262

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl (E)-3-(3-benzyloxy-1-phenyl-1H-pyrazol-4-yl)propenoateHCID 86591670—
CatalystHCID 178418390HCID 178418390—
SolventTetrahydrofuranHCID 8028—
Productethyl 3-(3-benzyloxy-1-phenyl-1H-pyrazol-4-yl)propionateHCID 2293066989%

Reaction Steps

A mixture of ethyl (E)-3-(3-benzyloxy-1-phenyl-1H-pyrazol-4-yl)propenoate (2.70 g), 5% palladium-carbon (3.00 g) and tetrahydrofuran (100 ml) was stirred under a hydrogen atmosphere at room temperature for 3 hrs. Palladium-carbon was filtered off and the filtrate was concentrated. The obtained crystals were collected by filtration to give ethyl 3-(3-benzyloxy-1-phenyl-1H-pyrazol-4-yl)propionate (1.78 g, yield 89%), which was then recrystallized from ethyl acetate-hexane. melting point: 123–124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241785B2
Source datasetuspto-grants-2007_07
ORD IDord-6d5d5152a62b4a5aae7e175a3dd765a4
Source noteuspto-grants-2007_07