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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178107Generated: October 27, 2026

Sodium Carbonate → 4-Phenyl-1-(triphenylmethyl)-1H-pyrazole

https://huagongshe.com/reaction/1178107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
Reactant4-Iodo-1-(triphenylmethyl)-1H-pyrazoleHCID 15324479—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventToluene waterHCID 22272177—
Product4-Phenyl-1-(triphenylmethyl)-1H-pyrazoleHCID 5955962048.38%

Reaction Steps

Na2CO3 (146 mg, 1.37 mmol) was added to a stirred solution of 4-iodo-1-trityl-1H-pyrazole (300 mg, 0.69 mmol) in toluene: H2O (5:1, 11.5 mL). Pd (PPh3)4 (80 mg, 0.07 mmol) and phenylboronic acid (126 mg, 1.03 mmol) were then added and the reaction mixture was heated to reflux for 2 hrs. The reaction mixture was then diluted with water and the product was extracted with ethyl acetate. The organic layer was washed with saturated brine solution, dried over sodium sulphate and concentrated to get the residue. The residue obtained was purified by column chromatography (using silica gel of 60-120 mesh and 5% EtOAc in Hexane as eluent) afford 120 mg (48.38% yield) of 4-phenyl-1-trityl-1H-pyrazole. 1H NMR (CDCl3): δ 7.96-7.94 (s, 1H), 7.64-7.6 (s, 1H), 7.46-7.4 (d, 2H), 7.36-7.0 (m, 1H), 7.24-7.16 (m, 7H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842696B2
Source datasetuspto-grants-2010_11
ORD IDord-e1febe7ef4dd42d7bfefe2fe8e1ed167
Source noteuspto-grants-2010_11