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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386348Generated: October 26, 2026

Dimethyl 1-trityl-3,5-pyrazoledicarboxylate → 1-Trityl-3,5-bis(hydroxymethyl)pyrazole

https://huagongshe.com/reaction/386348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl 1-trityl-3,5-pyrazoledicarboxylateHCID 12377531—
ReactantAluminium lithium hydrideHCID 21226445—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1-Trityl-3,5-bis(hydroxymethyl)pyrazoleHCID 1237753290%

Reaction Conditions

Temperature22.5 °C

Reaction Steps

To a solution of dimethyl 1-trityl-3,5-pyrazoledicarboxylate (3.200 g, 7.50 mmol) in dry THF (50 mL) were added 30 mL of 1.0 M LiAlH4 in Et2O. The resulting solution was stirred for about 16 h at room temperature (20-25° C.). After this time, the reaction was quenched by the slow addition of 1 mL of distilled water, followed by addition of 1 mL of 10% NaOH and 2.4 mL of water. The solids formed were removed by filtration, and 50 mL of dichloromethane was added to the filtrate. The organic phase was separated, washed with distilled water and a white microcrystalline solid was obtained after evaporation of the solvent under vacuum. Yield: 90% (2.843 g, 6.71 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372379B2
Source datasetuspto-grants-2013_02
ORD IDord-289c35bd6a904647ac68e4a575b46df0
Source noteuspto-grants-2013_02