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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Magnesium perchlorate | HCID 24840 | — |
| Reactant | (3-Phenyloxiranyl)methanol | HCID 89553 | — |
| Reactant | 4-methoxy-2,3-dihydro-1H-indole | HCID 16244441 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | 2-Hydroxy-3-(4-methoxyindolin-1-yl)-3-phenylpropanol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06448284B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-fba1dbd9606b4768b5f2bb98b07bc2bb |
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| Source note | uspto-grants-2002_09 |
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