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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15784Generated: October 25, 2026

Pyrazole → [3-(1H-Pyrazol-1-yl)phenyl]acetic acid

https://huagongshe.com/reaction/15784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantDodecaneHCID 8182—
ReactantCesium carbonateHCID 10796—
ReactantSodium HydroxideHCID 14798—
Reactant1,2-Diaminocyclohexane, trans-HCID 43806—
Reactant(3-Bromophenyl)acetic acidHCID 74653—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product[3-(1H-Pyrazol-1-yl)phenyl]acetic acidHCID 2106267165%

Reaction Steps

Pyrazole (1.2 eq), Cs2CO3 (2.5 eq), CuI (0.5 eq), trans-1,2-cyclohexanediamine (0.6 eq) and dodecane (1 eq), were added to a stirred solution of 3-bromophenylacetic acid (1 eq) in dioxane at room temperature under an inert atmosphere. The mixture was irradiated in a microwave reactor (PersonalChemistry Emrys™ Optimiser, 300 W, 160° C., 20 min), then added to a 1N aqueous solution of NaOH, and extracted with Et2O. The aqueous phase was acidified to pH=3 with HCl 2N, then extracted with ethyl acetate; this phase was washed with brine, dried over Na2SO4 and the solvent was removed under reduced pressure. The crude material was purified on SPE cartridge (Silica) eluting with a gradient from Cyclohexane/ethyl acetate 8:2, to Cyclohexane/ethyl acetate 1:1, affording the title compound in 65% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732600B2
Source datasetuspto-grants-2010_06
ORD IDord-0a2d14e5ae3c4320bcb0991c6c6eb791
Source noteuspto-grants-2010_06