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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395646Generated: November 3, 2026

4-bromo-3-(2-fluoro-5-methoxy-4-nitrophenyl)-1-methyl-5-(trifluoromethyl)-1H-pyrazole → HCID 19436747, compound

https://huagongshe.com/reaction/2395646

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-bromo-3-(2-fluoro-5-methoxy-4-nitrophenyl)-1-methyl-5-(trifluoromethyl)-1H-pyrazoleHCID 15278577—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
ProductHCID 19436747HCID 1943674783%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 3.16 g (7.9 mmole) 4-bromo-3-(2-fluoro-5-methoxy-4-nitrophenyl)-1-methyl-5-(trifluoromethyl)-1H-pyrazole in 59 mL acetic acid was heated to 80° C. under a nitrogen atmosphere. The heat and nitrogen were removed and 1.76 g (31.6 mmole) iron powder was added in 3 portions over 5 min. The solution was stirred at 80° C. for an additional 30 min. The solution was cooled and filtered through Celite®. The filtrate was diluted with 100 mL water and extracted three times with diethyl ether. The ether extracts were washed with brine, dried over anhydrous MgSO4, and concentrated in vacuo. The residue was purified chromatographically using 40% ethyl acetate in hexane as the eluent to give 2.4 g (83%) of 4-(4-bromo-1-methyl-5-(trifluoromethyl)-1H-pyrazol-3-yl)-5-fluoro-2-methoxy-benzeneamine as a white solid, mp 85°-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489571
Source datasetuspto-grants-1996_02
ORD IDord-2efdad4ada724362b9c8cef1c69859e3
Source noteuspto-grants-1996_02