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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570077Generated: October 25, 2026

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

https://huagongshe.com/reaction/570077

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 numberUS09023315B2
Source datasetuspto-grants-2015_05
ORD IDord-874d4b630d024c3a9876189974d5a211
Source noteuspto-grants-2015_05