Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 475266Generated: October 29, 2026

4-Bromo-1H-indole-3-carbaldehyde → 4-Bromo-3-methyl-1H-indole

https://huagongshe.com/reaction/475266

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1H-indole-3-carbaldehydeHCID 2763178—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product4-Bromo-3-methyl-1H-indoleHCID 5298770475.3%

Reaction Steps

To a refluxing solution of 4-bromo-1H-indole-3-carbaldehyde (644 mg, 2.87 mmol) in dry THF (20 mL) was added LiAlH4 (218 mg, 5.75 mmol) in several small portions. Heating at reflux was continued for 1 h, the reaction cooled to RT and quenched with water (220 μL), 15% aq. NaOH (w/w, 220 μL), and water (650 μL). The resulting precipitate was filtered and the filtrate was concentrated under reduced pressure to dryness. To the residue was added aq. NaOH (10 mL) and the solution twice extracted with DCM (2×10 mL). The combined extracts were dried (MgSO4), filtered and concentrated in vacuo to afford 454 mg (75%) of 4-bromo-3-methyl-1H-indole (230) as light brown oil: MS (ESI) m/z=210.1 [M+1]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637537B2
Source datasetuspto-grants-2014_01
ORD IDord-272d18d441bf4f5abccf56b9955905a0
Source noteuspto-grants-2014_01