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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524638Generated: November 4, 2026

Water → 3-Buten-2-ol, 1-(triphenylmethoxy)-, (2S)-

https://huagongshe.com/reaction/1524638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHexaneHCID 8058—
ReactantTrimethylsulfonium iodideHCID 75127—
Reactant(S)-Glycidyl Trityl EtherHCID 7168113—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product3-Buten-2-ol, 1-(triphenylmethoxy)-, (2S)-HCID 11484468—

Reaction Conditions

Temperature-20 °C

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 min, (S)-trityl glycidyl ether (50.0 g) was added at the same temperature, and the mixture was stirred at RT for 30 min. Water was added to the reaction solution, followed by extraction with diethyl ether. The organic layer was dried over anhydrous MgSO4. 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). 1H-NMR (400 MHz, CDCl3) δ (ppm): 3.09-3.13 (m, 1H), 3.20-3.23 (m, 1H), 4.26-4.29 (m, 1H), 5.14-5.32 (m, 2H), 5.76-5.84 (m, 1H), 7.23-7.45 (m, 15H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079914B2
Source datasetuspto-grants-2015_07
ORD IDord-f7ecd8de211f4c9392882321ae70bc08
Source noteuspto-grants-2015_07