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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1634097Generated: October 26, 2026

Ethyl Acetoacetate → 1-(4'-Nitrophenyl)-5-(2-triisopropylsilylethynyl)-3-methylpyrazole

https://huagongshe.com/reaction/1634097

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetoacetateHCID 8868—
ReactantPhosphorus tribromideHCID 24614—
Reactant(Triisopropylsilyl)acetyleneHCID 2734682—
Reactant1-(4'-Nitrophenyl)-5-bromo-3-methylpyrazoleHCID 11482930—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
SolventTriethylamineHCID 8471—
Product1-(4'-Nitrophenyl)-5-(2-triisopropylsilylethynyl)-3-methylpyrazoleHCID 1867711895%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 1-(4′-nitrophenyl)-5-bromo-3-methylpyrazole (prepared as described for Example 19 except using ethyl acetoacetate instead of ethyl trifluoroacetoacetate and using PBr3 in acetonitrile and refluxing for 72 hr for the halogenation step) (100 mg, 0.35 mmol) in triethylamine (5 mL) was added Pd(PPh3)4 (20 mg, 0.017 mmol) and CuBrSMe2 (8 mg, 0.036 mmol), followed by triisopropylsilylacetylene (72 mg, 0.39 mmol). The mixture was heated to 70° C. for 1 hour and cooled to room temperature. The solid was filtered off and the filtrate was concentrated. The residue was purified by column chromatography on silica gel (hexane/acetate, 4:1) to give the title compound (127 mg, 95%). mp: 71-73° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06506747B1
Source datasetuspto-grants-2003_01
ORD IDord-6b371fe8f2ef49e7aa353d0e8740e369
Source noteuspto-grants-2003_01