Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (R)-1,2-Epoxypropane | HCID 146261 | — |
| Reactant | 5-Fluoro-3-methyl-1H-indole-2-carboxylic acid | HCID 1132967 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53945475 | HCID 53945475 | 70% |
Reaction Steps
A suspension of 1.16 g of 5-fluoro-3-methyl-indole-2-carboxylic acid in 16 ml of diphenyl ether was stirred at 260° for 5 hours and, after cooling to 0°, diluted with 30 ml of tetrahydrofuran. 225 mg of sodium hydride dispersion were added and the mixture was stirred for one hour. Subsequently, 0.63 ml of (R)-methyloxirane was added and the reaction mixture was stirred at room temperature for 90 hours. The mixture was extracted with diethyl ether, water and saturated sodium chloride solution and the organic phase was dried over sodium surfate. The solvent was removed and the residue was chromatographed over 120 g of silica gel with hexane-toluene (1:1) and subsequently with toluene-ethyl acetate (19:1). 0.87 g (70%) of (R)-1-(5-fluoro-3-methylindol-1-yl)-propan-2-ol was obtained as a pale brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05494928 |
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| Source dataset | uspto-grants-1996_02 |
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| ORD ID | ord-016a5262032b43d0ab7f5ad734611c42 |
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| Source note | uspto-grants-1996_02 |
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