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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 884606Generated: October 26, 2026

Boron tribromide → 4-methyl-1H-indol-5-ol

https://huagongshe.com/reaction/884606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron tribromideHCID 25134—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Methoxy-4-methylindoleHCID 3296242—
SolventDichloromethaneHCID 6344—
Product4-methyl-1H-indol-5-olHCID 21691244—

Reaction Conditions

Temperature0 °C

Reaction Steps

5-Methoxy-4-methyl-1H-indole (10 g, 62.0 mmol) is dissolved in DCM (400 mL) and cooled to 0° C. BBr3 (155 mL, 155 mmol) is added dropwise over 1 hour and the black mixture is allowed to warm to room temperature overnight (17 hours). The reaction is poured over a mixture of ice and sodium bicarbonate (aq) solution and extracted with ethyl acetate (1.5 L) and concentrated to a black oil. The oil is absorbed onto silica and separated via FCC (0-50% ethyl acetate:heptanes) to obtain the title compound as a solid. MS (ESI) m/z 148.23 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08242125B2
Source datasetuspto-grants-2012_08
ORD IDord-eb033c993c2b4fab8457a4c77ea3ca8c
Source noteuspto-grants-2012_08