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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylindoleHCID 7224—
Reactant4-(5-Fluoro-2-methoxyphenyl)-4-methylpentan-2-oneHCID 22284922—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Fluoro-2-methoxyphenyl)-2-(indol-2-ylmethyl)-4-methylpentan-2-olHCID 2239852631.2%

Reaction Conditions

Temperature-20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08212040B2
Source datasetuspto-grants-2012_07
ORD IDord-c38237a653f346d09984409fb17f7c58
Source noteuspto-grants-2012_07