HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510893Generated: October 26, 2026
2-Methylindole → 4-(5-Fluoro-2-methoxyphenyl)-2-(indol-2-ylmethyl)-4-methylpentan-2-ol
https://huagongshe.com/reaction/1510893
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methylindole | HCID 7224 | — |
| Reactant | 4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-one | HCID 22284922 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(5-Fluoro-2-methoxyphenyl)-2-(indol-2-ylmethyl)-4-methylpentan-2-ol | HCID 22398526 | 31.2% |
Reaction Steps
To a solution of 2-methylindole (130 mg) in THF (2 mL) stirred under argon cooled on dry ice/acetone was added n-butyl lithium (2M in pentane, 1.6 mL). After 2 minutes, potassium tert-butoxide (1M in THF, 2 mL) was added and the mixture was allowed to warm to approximately −20° C. After 5 minutes, precipitate was noted and the mixture was cooled to −70° C. 4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-one (Example 17) (440 mg) in THF (1.5 mL) was added all at once. The cooling bath was removed and the mixture was stirred for 10 minutes and then quenched with EtOH (0.5 mL). The mixture was diluted with EtOAc, washed with water, dried, filtered, and evaporated. Chromatography over silica gel (EtOAc-hexanes (1:9)) gave product which solidified on trituration with hexanes-ether. The solid was recrystallized from ether-hexanes, collected by filtration and dried under vacuum to give 0.11 g of the title compound, m.p. 118° C.-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08212040B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-c38237a653f346d09984409fb17f7c58 |
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| Source note | uspto-grants-2012_07 |
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