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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441092Generated: October 25, 2026

4-Methylindole → 4-Methylindoline

https://huagongshe.com/reaction/441092

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylindoleHCID 85282—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
Product4-MethylindolineHCID 58370392.2%

Reaction Steps

To a solution of 4-methylindole (7.433 g, 0.0567 mol) in 100 mL of glacial acetic acid was added NaCNBH3 (7.25 g, 0.12 mol) portionwise over 1.5 h. The reaction mixture was then concentrated in vacuo, water was added and the solution was basified with 10N NaOH. The resulting mixture was extracted with ethyl acetate (×3) and the organic extract was washed (brine), dried (Na2SO4) and evaporated to give an oil. Flash chromatography (SiO2 /ethyl acetate-hexane, 1:4) of this oil gave pure 4-methylindoline (6.962 g, 92%) as an oil: 1H NMR (DMSO-d6, 200 MHz) δ 6.78 (t, J=7.6 Hz, 1H), 6.33 (d, J=7.4 Hz, 1H), 6.30 (d, J=7.6 Hz, 1H), 5.36 (br s, 1H), 3.38 (t, J=8.5 Hz, 2H), 2.81 (t, J=8.5 Hz, 2H), 2.11 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05521188
Source datasetuspto-grants-1996_05
ORD IDord-7053962630f64b87922abe59ece4e47e
Source noteuspto-grants-1996_05