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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 83515Generated: October 26, 2026

1-Phenyl-5-(3-propylphenyl)-4,5-dihydro-1H-pyrazol-3-ylamine → 1-Phenyl-5-(3-propylphenyl)-1H-pyrazol-3-ylamine

https://huagongshe.com/reaction/83515

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Phenyl-5-(3-propylphenyl)-4,5-dihydro-1H-pyrazol-3-ylamineHCID 71287742—
SolventTolueneHCID 1140—
Product1-Phenyl-5-(3-propylphenyl)-1H-pyrazol-3-ylamineHCID 7128773947%

Reaction Steps

To a solution of the crude product of 1-phenyl-5-(3-propylphenyl)-4,5-dihydro-1H-pyrazol-3-ylamine (18.6 g) in toluene (185 ml) was added activated carbon (pH5 to 8, 9.29 g), and the mixture was stirred overnight under oxygen atmosphere at reflux. This reaction solution was cooled to room temperature, and then the activated carbon was filtered off through Celite, and eluted with ethyl acetate. This filtrate was concentrated under reduced pressure, the resulting residue was dissolved in toluene (185 ml), and to the solution was added fresh activated carbon (pH5 to 8, 9.29 g), and the mixture was stirred overnight under oxygen atmosphere at reflux. This reaction solution was cooled to room temperature, and then the activated carbon was filtered off through Celite, and eluted with ethyl acetate. This filtrate was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=4/1 to 1/1) to give the titled compound (8.68 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846746B2
Source datasetuspto-grants-2014_09
ORD IDord-dddac6624c50444c99b32e387ba30678
Source noteuspto-grants-2014_09