HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyrazole → HCID 68531009, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 68527721 | HCID 68527721 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68531009 | HCID 68531009 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08372379B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-40163fd5f924425a82e66549e68745a3 |
| Source note | uspto-grants-2013_02 |