HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80307Generated: October 28, 2026
Trityl chloride → HCID 58455161, compound
https://huagongshe.com/reaction/80307
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (R)-3-Pyrrolidinol | HCID 2759337 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 58455161 | HCID 58455161 | 62% |
Reaction Steps
(R)-(+)-3-Pyrrolidinol (1.0 g, 11.5 mmol) (Aldrich) and triphenylchloromethane (1.00 g, 3.59 mmol) (Wako Pure Chemical Industries, Ltd.) were dissolved in acetonitrile (30 mL) (Wako Pure Chemical Industries, Ltd.), and the mixture was refluxed for 3 hours. The mixture was allowed to cool to room temperature, and then a saturated aqueous solution of sodium hydrogen carbonate (Wako Pure Chemical Industries, Ltd.) was added to the reaction solution, followed by extraction with ethyl acetate (Wako Pure Chemical Industries, Ltd.). The organic layer was dried with anhydrous sodium sulfate (Wako Pure Chemical Industries, Ltd.), and the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (chloroform (Wako Pure Chemical Industries, Ltd.) as an eluent), to thereby obtain the title compound (0.73 g, 62% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846012B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-17b6ac906b664eaa906937820473dd72 |
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| Source note | uspto-grants-2014_09 |
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