반응 #657260
ord-00b71c285b6a4174b22690b450dfd9e6
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시약
반응 조건
후처리
- 1기타The synthesis of this compound
- 2기타After removal of the solvent under vacuum
- 3세척the resulting residue was washed with distilled water, n-hexane
- 4기타finally dried under vacuum
실험 절차
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).