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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279493Generated: October 26, 2026

Magnesium perchlorate → 2-Hydroxy-3-(4-methoxyindolin-1-yl)-3-phenylpropanol

https://huagongshe.com/reaction/1279493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMagnesium perchlorateHCID 24840—
Reactant(3-Phenyloxiranyl)methanolHCID 89553—
Reactant4-methoxy-2,3-dihydro-1H-indoleHCID 16244441—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
Product2-Hydroxy-3-(4-methoxyindolin-1-yl)-3-phenylpropanolHCID 18428416—

Reaction Steps

A solution of 1.00 g (6.62 mmol) of 4-methoxyindoline (Gangjee et al., J. Med. Chem. 1997, 40, 479-485) and 1.90 g (8.51 mmol) of magnesium perchlorate in 20 mL of CH3CN was treated in a dropwise manner with a solution of 1.00 g (6.62 mmol) of 2,3-epoxy-3-phenyl-1-propanol (Ogata and Tomizawa, Bull. Chim. Soc. Jap. 1977, 50, 261-265) in 10 mL of CH3CN. The reaction was stirred at ambient temperature for 2.5 hours and was diluted with 30 mL of saturated aqueous NaHCO3. The organic layer was separated and the aqueous phase was extracted with EtOAc (2×20 mL). The combined organic layers were dried (Na2SO4), filtered, and concentrated in vacuo. The oil was purified by radial chromatography (SiO2; 10% then 20% then 30% EtOAc in hexanes) to afford 1.55 g (5.17 mmol; 78%) of the subtitled compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06448284B1
Source datasetuspto-grants-2002_09
ORD IDord-fba1dbd9606b4768b5f2bb98b07bc2bb
Source noteuspto-grants-2002_09