HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373471Generated: October 30, 2026
Aluminium lithium hydride → HCID 21964288, compound
https://huagongshe.com/reaction/2373471
Participants
| Role | Name | HCID | Charge |
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| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 21964300 | HCID 21964300 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 21964288 | HCID 21964288 | 86.2% |
Reaction Steps
Lithium aluminum hydride (0.244 g, 6.1 mmol) was added portionwise to a stirring solution of ethyl 1-(4-methylbenzyl)-5-[4-(trifluoromethoxy)phenyl]-1H-indole-2-carboxylate (2.0 g, 4.4 mmol) in ethyl ether (17 mL) at 0° C. under a nitrogen atmosphere over a period of 5 minutes. The mixture was then warmed up to room temperature. After the reaction mixture was stirred at room temperature for 5 hours, the reaction was carefully quenched with water and filtered. The filtrate was extracted with ethyl acetate. The organic extract was washed with water and brine, dried over anhydrous magnesium sulfate and evaporated to afford the title compound as a white solid (1.56 g, 86%). Mass spectrum (ESI, [M+H]+) m/z 412. 1HNMR (400 MHz, DMSO-d6): δ 7.81 (s, 1H), 7.76 (d, 2H, J=6.71 Hz), 7.45-7.35 (m, 4H), 7.08 (d, 2H, J=7.74 Hz), 6.96 (d, 2H, J=8.09 Hz), 6.50 (s, 1H), 5.44 (s, 2H), 5.35 (t, 1H), 4.60 (d, 2H), and 2.23 ppm (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07459478B2 |
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| Source dataset | uspto-grants-2008_12 |
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| ORD ID | ord-c71b8c5b315846d3ab10f10199fe98e9 |
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| Source note | uspto-grants-2008_12 |
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