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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595298Generated: October 30, 2026

Methyl 4-acetylbenzoate → methyl 4-[1-hydroxy-1-(1-trityl-1H-pyrazol-4-yl)ethyl]benzoate

https://huagongshe.com/reaction/595298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-acetylbenzoateHCID 137990—
Reactant4-Bromo-1-trityl-1H-pyrazoleHCID 10834188—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Productmethyl 4-[1-hydroxy-1-(1-trityl-1H-pyrazol-4-yl)ethyl]benzoateHCID 118208817—

Reaction Conditions

Temperature-78 °C

Reaction Steps

n-BuLi (1.65 mL, 4 mmol) was added dropwise to a mixture of 4-bromo-1-trityl-1H-pyrazole (1.5 g, 3.8 mmol) in THF (15 mL) cooled to −78° C. Then the mixture was stirred at −78° C. for 1 hour. After methyl 4-acetylbenzoate (0.71 g, 3.8 mmol) in THF (1 mL) was added, the mixture was stirred at −78° C. for 2 hours, and then quenched with saturated aqueous ammonium chloride solution. The mixture was extracted with ethyl acetate. The organic layer was concentrated and the residue was purified by chromatography on silica gel to afford methyl 4-[1-hydroxy-1-(1-trityl-1H-pyrazol-4-yl)ethyl]benzoate. MS ESI calc'd. for C32H29N2O3 [M+H]+ 489. found 489.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242984B2
Source datasetuspto-grants-2016_01
ORD IDord-d56f52b979d54fcdaac4de9e075b4f75
Source noteuspto-grants-2016_01