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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382041Generated: November 1, 2026

Ammonium Chloride → 4-(5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-ol

https://huagongshe.com/reaction/2382041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(5-Fluoro-1h-indol-3-yl)butan-2-oneHCID 22662931—
ReactantHCID 178418689HCID 178418689—
SolventTetrahydrofuranHCID 8028—
Product4-(5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-olHCID 6855908326%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-(5-fluoro-1H-indol-3-yl)-butan-2-one (11.1 g, 54.1 mmol) in THF (200 mL) at 0° C. is treated with MeMgBr (54.1 mL, 3 M in THF, 162.3 mmol) and stirred at 0° C. for 2 h, and warmed to rt overnight. The mixture is then poured over ice, treated with solid NH4Cl (3 g), and extracted with EtOAc (3×120 mL). The combined organic layer is dried (Na2SO4), filtered and concentrated in vacuo. The residue is purified by silica gel chromatography eluting with 10%-60% EtOAc in heptane to afford 4-(5-fluoro-1H-indol-3-yl)-2-methyl-butan-2-ol (3.07 g, 26%). MS: 222 (M+H); 1H NMR (300 MHz, CDCl3): δ 7.94 (s, NH, 1H), 7.22 (m, 2H), 7.03 (s, 1H), 6.93 (m, 1H), 2.81 (m, 2H), 1.90 (m, 2H), 1.33 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08258130B2
Source datasetuspto-grants-2012_09
ORD IDord-7402002e2a7749bc9ccfeb4170820c99
Source noteuspto-grants-2012_09