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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816852Generated: November 1, 2026

Indole → 5-Fluoroindole

https://huagongshe.com/reaction/1816852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
Reactant3-Methyl-2-butanoneHCID 11251—
Reactant4-Fluorophenylhydrazine hydrochlorideHCID 69981—
SolventAcetic AcidHCID 176—
Product5-FluoroindoleHCID 6786199.9%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture containing 4-Fluorophenylhydrazine hydrochloride (5.0 g; 30.75 mmol; ALDRICH), 3-methyl-2-butanone (3.7 g; 43 mmol; ALDRICH) and acetic acid (30 ml) was stirred for 30 min. under nitrogen to obtain the clear solution. The mixture was then refluxed at 130° C. The appearance of UV-Vis Abs. Max at 255 nm and the disappearance of the peak at 282 nm confirmed the formation of the indole. At the end of 40 min. the reaction was stopped and the mixture was poured into crushed ice (100 g). The residue was extracted into ethyl acetate (100 ml×2), washed with water (100 ml×2) and ethyl acetate layer was dried over anhydrous sodium sulfate. After filtration, ethyl acetate was removed, and the residue was dried to give 4.15 g of the indole (Yield 76%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07597878B2
Source datasetuspto-grants-2009_10
ORD IDord-43fda37918a649d2b0247493b9929c3c
Source noteuspto-grants-2009_10