Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | (2S)-2-Methyloxirane | HCID 146262 | — |
| Reactant | HCID 18986211 | HCID 18986211 | — |
| Solvent | Diphenyl Ether | HCID 7583 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53763671 | HCID 53763671 | 35.5% |
Reaction Steps
A suspension of 0.8 g of 5-fluoro-4-trifluoromethylindole-2-carboxylic acid in 16 ml of diphenyl ether was stirred at 260° for 4 hours and, after cooling to 0°, diluted with 16 ml of tetrahydrofuran. 122 mg of sodium hydride dispersion were added and the mixture was stirred for 1 hour. Subsequently, 0.46 ml of (S)-methyloxirane was added and the reaction mixture was stirred at room temperature for 60 hours. The mixture was extracted with diethyl ether, water and saturated sodium chloride solution and the organic phase was dried over sodium sulfate. The solvent was removed and the residue was chromatographed over 40 g of silica gel with hexane-toluene (1:1) and subsequently with toluene-ethyl acetate (15:1). There was obtained 0.3 g (35.5%) of (R)-1-(5-fluoro-4-trifluoromethyl-indol-1-yl)-propan-2-ol as light brown crystals.
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-d6d4ee46f7b2403f92b0e0b063c62e93 |
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| Source note | uspto-grants-1996_02 |
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