HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indole-2-carbaldehyde → (E)-5-[3-(4-Fluorophenyl)-1-isopropyl-1H-indol-2-yl]-3-oxopent-4-enoic Acid Ethyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Fluorophenyl)-1-(1-methylethyl)-1H-indole-2-carbaldehyde | HCID 11312061 | — |
| Reactant | 3-Oxo-4-(triphenylphosphoranylidene)butanoate | HCID 18457748 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (E)-5-[3-(4-Fluorophenyl)-1-isopropyl-1H-indol-2-yl]-3-oxopent-4-enoic Acid Ethyl Ester | HCID 20730393 | — |
Reaction Steps
The ylide 3-oxo-4-(triphenylphosphoranylidene)butanoate (5.0 g, 12.8 mmol) is solved under argon atmosphere in 100 ml acetonitrile. Under vigorous stirring 3-(4-Fluoro-phenyl)-1-isopropyl-1H-indole-2-carbaldehyde (4.2 g, 10.7 mmol) is added in 5 portions and then heated to reflux. After 50 h the reaction is cooled to room temperature. The slight brown solvent is evaporated and the residue is dried under vacuum to obtain a brown waxy oil. Chromatography over silica gel with hexane:ethylacetate (4:1/v:v) give a yellow oil of (E)-5-[3-(4-Fluoro-phenyl)-1-isopropyl-1H-indol-2-yl]-3-oxo-pent-4-enoic acid ethyl ester. MS: 393.46
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07208623B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-2c1a5c9e6d16422bb69ba5bb16e8c048 |
| Source note | uspto-grants-2007_04 |