HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566238Generated: October 31, 2026
Trityl chloride → HCID 15475336, compound
https://huagongshe.com/reaction/566238
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(1H-Pyrazol-4-yl)ethanol | HCID 4293604 | — |
| Reactant | HCID 178520322 | HCID 178520322 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 15475336 | HCID 15475336 | — |
| Product | 2-[1-(Triphenylmethyl)-1H-pyrazol-4-yl]ethan-1-ol | HCID 15475337 | — |
Reaction Steps
A mixture of 2-(3-pyrazolyl)ethanol and 2-(4-pyrazolyl)ethanol (2.4:1) (2.50 g) was dissolved in DMF (30 ml). To the solution were added, while stirring, triethylamine (2.26 g) and trityl chloride (6.22 g). The mixture was stirred at 25° C. for one hour, then at 40° C. for one hour. The reaction mixture was diluted with water, which was subjected to extraction with ethyl acetate. The organic layer was washed with an aqueous saline solution, which was dried over anhydrous magnesium sulfate, followed by concentration under reduced pressure. The concentrate was purified by means of a column chromatography (carrier: silica gel, 300 g, developing solvent: ethyl acetate-hexane, 1:1) to afford 2-(1-triphenylmethyl-3-pyrazolyl)ethanol (3.75 g) and 2-(1-triphenylmethyl-4-pyrazolyl)ethanol (1.42 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174877B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-5eb0e8ee898c4b9293039966ec2b7b64 |
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| Source note | uspto-grants-2001_01 |
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