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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12625Generated: October 30, 2026

Ammonium Chloride → (7-bromo-1-methyl-1H-indol-2-yl)methanol

https://huagongshe.com/reaction/12625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium borohydrideHCID 4148881—
Reactantethyl 7-bromo-1-methyl-1H-indole-2-carboxylateHCID 68693640—
SolventTetrahydrofuranHCID 8028—
Product(7-bromo-1-methyl-1H-indol-2-yl)methanolHCID 68695245—

Reaction Steps

To a tetrahydrofuran (40 mL) solution of ethyl 7-bromo-1-methyl-1H-indole-2-carboxylate (1.99 g), lithium tetrahydroborate (463 mg) was added at 0° C., followed by stirring at room temperature for 5 hours. To the reaction mixture, an aqueous saturated ammonium chloride solution was added, followed by extraction with ethyl acetate. The organic layer was washed in turn with water and saturated saline, dried over anhydrous sodium sulfate and then concentrated. The residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=90:10-70:30) to obtain the titled compound having the following physical properties (880 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728023B2
Source datasetuspto-grants-2010_06
ORD IDord-502f3206842346ae9fee5bc68ef8a314
Source noteuspto-grants-2010_06