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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349548Generated: October 30, 2026

Trityl chloride → 1-(2-Triphenylmethyloxyethyl)-5-aminopyrazole-4-carbaldehyde

https://huagongshe.com/reaction/349548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrityl chlorideHCID 6456—
Reactant5-amino-1-(2-hydroxyethyl)-1H-pyrazole-4-carbaldehydeHCID 17962034—
SolventPyridineHCID 1049—
Product1-(2-Triphenylmethyloxyethyl)-5-aminopyrazole-4-carbaldehydeHCID 1796196161%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of 5-amino-1-(2-hydroxyethyl)-1H-pyrazole-4-carbaldehyde (40.2 g) in pyridine (400 ml) was added triphenylmethyl chloride (86.7 g) at room temperature. The mixture was stirred at 60° C. for 5 hours. The reaction mixture was evaporated under reduced pressure and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, filtered, and evaporated in vacuo. The residue was purified by column chromatography on silica gel eluting with ethyl acetate/hexane (3:2) to give 5-amino-1-(2-triphenylmethyloxyethyl)-1H-pyrazole-4-carbaldehyde (62.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179801B2
Source datasetuspto-grants-2007_02
ORD IDord-457674367d9646c887961f2cdeacad81
Source noteuspto-grants-2007_02