Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 1-Phenethylamine, (+)- | HCID 643189 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(1,5-dimethyl-1H-pyrazol-4-yl)ethanone | HCID 7019427 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67183847 | HCID 67183847 | 41% |
Reaction Steps
1-(1,5-Dimethyl-1H-pyrazol-4-yl)ethanone (J. Heterocyclic Chem. 1986, 23, 275-279, 4.82 g, 34.9 mmol) and (R)-1-Phenylethylamine (5.07 g, 41.9 mmol) in Titanium tetraisopropoxide (22.1 g, 77.7 mmol) were stirred at room temperature for 16 hours. Ethanol (30 ml) and THF (30 ml) were added at −20° C., then Sodium borohydride (3.96 g, 105 mmol) was added at −20° C. then the whole mixture was stirred for 3 h whilst warming to room temperature. The reaction was quenched with water (20 ml) and diluted with ethyl acetate-THF. Then the mixture was filtered through celite and washed with ethyl acetate. The filtrate was dried over Na2SO4, concentrated and purified by silica gel column chromatography eluted with ethyl acetate/n-Hexane=2/1 to 100/0 to furnish the title compound (3.44 g, 41% yield) as colorless oil. 1H NMR (270 MHz, CDCl3) δ 1.26 (3H, d, J=6.6 Hz), 1.27 (3H, d, J=6.6 Hz), 1.96 (3H, s), 3.44 (1H, q, J=6.6 Hz), 3.60 (1H, q, J=6.6 Hz), 3.76 (3H, s), 7.20-7.38 (6H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964732B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-c36e33100e8d4fc5beb228eb453fdb98 |
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| Source note | uspto-grants-2011_06 |
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