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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53151Generated: October 25, 2026

4-Methylindole → 4-Methylindoline

https://huagongshe.com/reaction/53151

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) δ6.78 (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 numberUS05618816
Source datasetuspto-grants-1997_04
ORD IDord-018dd87bdd534d888b93dd1b102cb8bb
Source noteuspto-grants-1997_04