HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842220Generated: November 2, 2026
Water → 3-Buten-2-ol, 1-(triphenylmethoxy)-, (2S)-
https://huagongshe.com/reaction/1842220
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Trimethylsulfonium iodide | HCID 75127 | — |
| Reactant | (S)-Glycidyl Trityl Ether | HCID 7168113 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Buten-2-ol, 1-(triphenylmethoxy)-, (2S)- | HCID 11484468 | — |
Reaction Steps
A solution of n-BuLi in hexane (2.6 M; 182 mL) was added dropwise to a solution of trimethylsulfonium iodide (96.8 g) in THF (800 mL) at −30° C. After stirring at −20° C. for 20 minutes, (S)-trityl glycidyl ether (50.0 g) was added at the same temperature, and the mixture was stirred at room temperature for 30 minutes. Water was added to the reaction solution, followed by extraction with diethyl ether. The organic layer was dried over anhydrous magnesium sulfate. The insoluble matter was separated by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound (52.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946210B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-bcdd65296c9e4045a21a68f7089bbd30 |
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| Source note | uspto-grants-2015_02 |
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