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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386349Generated: October 30, 2026

Pyrazole → HCID 68531009, compound

https://huagongshe.com/reaction/386349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrazoleHCID 1048—
ReactantTrityl chlorideHCID 6456—
ReactantSodium hydrideHCID 24758—
ReactantHCID 68527721HCID 68527721—
SolventDimethylformamideHCID 6228—
ProductHCID 68531009HCID 6853100990%

Reaction Steps

The synthesis of this compound was done by tritylation of trimethyl-3,4,5-pyrazoletricarboxylate (1680 mg, 6.94 mmol) using a procedure similar to the one described in examples 2 and 3 for the synthesis of other tritylated pyrazole derivatives. The starting pyrazole reacted with sodium hydride (405 mg, 10.13 mmol) in dry dimethylformamide (80 mL) for 30 min at room temperature. Then, trityl chloride (1935 mg, 6.94 mmol) was added and the reaction mixture stirred overnight at room temperature. After removal of the solvent under vacuum, the resulting residue was washed with distilled water, n-hexane, and finally dried under vacuum to afford the title compound, as a white microcrystalline solid. Yield: 90% (3.034 g, 6.26 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372379B2
Source datasetuspto-grants-2013_02
ORD IDord-40163fd5f924425a82e66549e68745a3
Source noteuspto-grants-2013_02