HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716694Generated: October 30, 2026
Ethanol → 3-(6-Methoxy-1H-Indol-4-yl)-3-phenyl-propionaldehyde
https://huagongshe.com/reaction/1716694
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diisobutylaluminum hydride | HCID 14487 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3-(6-Methoxy-1H-Indol-4-yl)-3-phenyl-propionic acid ethyl ester | HCID 59831728 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(6-Methoxy-1H-Indol-4-yl)-3-phenyl-propionaldehyde | HCID 59831913 | — |
Reaction Steps
To a −78° C. solution of 3-(6-Methoxy-1H-Indol-4-yl)-3-phenyl-propionic acid ethyl ester CXVII (0.39 g, 1.2 mmol) in DCM (10 ml) was added DIBALH (1M in hexane, 4.0 ml, 4.0 mmol). After stirring for 90 minutes at −78° C., more DIBALH (1M in hexane, 1.2 ml, 1.2 mmol) was added. The resulting mixture was stirred for 2.25 hours, after which EtOH (2 ml) and a saturated solution of NaHCO3 (2 ml) were added. The mixture was then stirred at room temperature for 30 min, filtered, and the filter cake was washed with EtOAc. The filtrate was concentrated and washed with a saturated solution of NaHCO3, dried over Na2SO4, filtered, concentrated, and purified via flash chromatography (hexane/EtOAc) affording 3-(6-Methoxy-1H-Indol-4-yl)-3-phenyl-propionaldehyde CXVIII as a colorless syrup (0.27 g, 82% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803830B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-c057ca2fb8a242988488dd7b8b63fcd5 |
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| Source note | uspto-grants-2010_09 |
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