Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096980Generated: October 27, 2026

Water → Methyl 3,5-diethoxy-4-(1-methyl-1H-pyrazol-4-yl)benzoate

https://huagongshe.com/reaction/1096980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
ReactantMethyl 4-bromo-3,5-diethoxybenzoateHCID 57930905—
CatalystHCID 178506421HCID 178506421—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 3,5-diethoxy-4-(1-methyl-1H-pyrazol-4-yl)benzoateHCID 57930985—

Reaction Conditions

Temperature90 °C

Reaction Steps

Methyl 4-bromo-3,5-diethoxybenzoate (1 g) and 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (895 mg) were dissolved in DME in a nitrogen atmosphere, and potassium phosphate (2.1 g) and 1,1′-bis(diphenylphosphino)ferrocene palladium (D) chloride-CH2Cl2 complex (269 mg) were added to it at room temperature, and degassed. The reaction liquid was stirred overnight at 90° C., then cooled to room temperature, and water was added to it, and this was filtered through Celite. The filtrate was extracted with chloroform, washed with saturated saline water, and dried with sodium sulfate. Sodium sulfate was removed through filtration, the filtrate was concentrated under reduced pressure, and the residue was purified through silica gel column chromatography (hexane/ethyl acetate=100/0 to 50/50 to 35/65) to obtain the title compound as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138197B2
Source datasetuspto-grants-2012_03
ORD IDord-27647d87145c4f04a979401548d5c6d7
Source noteuspto-grants-2012_03