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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499105Generated: November 2, 2026

Water → 1-[5-Bromo-2-(3-methyl-pyrazol-1-yl)-phenyl]-2,2,2-trifluoroethanone

https://huagongshe.com/reaction/1499105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant1-(5-Bromo-2-fluorophenyl)-2,2,2-trifluoroethan-1-oneHCID 11369266—
ReactantHCID 178428694HCID 178428694—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product1-[5-Bromo-2-(3-methyl-pyrazol-1-yl)-phenyl]-2,2,2-trifluoroethanoneHCID 117951914—

Reaction Conditions

Temperature110 °C

Reaction Steps

1-(5-bromo-2-fluorophenyl)-2,2,2-trifluoroethanone (2.20 g, 8.12 mmol) from Step 1, K2CO3 (1.68 g, 12.2 mmol), and 3-methyl-1H-pyrazole (1.33 g, 16.2 mmol) were stirred in toluene (10 mL). The reaction was then heated to 110° C. for 16 h. The reaction was cooled, and water and EtOAc were added. The toluene-EtOAc layer is removed in vacuo, and then the reaction is extracted with water and EtOAc, washed with brine, and dried over Na2SO4, filtered, and concentrated in vacuo. Purification by normal phase silica gel column chromatography (EtOAc/heptane) provided 1-[5-bromo-2-(3-methyl-pyrazol-1-yl)-phenyl]-2,2,2-trifluoroethanone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199994B2
Source datasetuspto-grants-2015_12
ORD IDord-ba0eb90c8b5b4e29b8fc87d2f423c604
Source noteuspto-grants-2015_12