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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890997Generated: November 1, 2026

Indole → HCID 12047551, compound

https://huagongshe.com/reaction/890997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantEthyl BromideHCID 6332—
ReactantAmmonium ChlorideHCID 25517—
ReactantMagnesiumHCID 5462224—
ReactantN-benzyloxymethyl-2,3-dibromomaleimideHCID 11122331—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12047551HCID 12047551—
ProductHCID 178418443HCID 178418443—

Reaction Steps

A solution of ethylmagnesium bromide is prepared, starting from magnesium (6.75 mmol) suspended in bromoethane (6.75 mmol) and dry tetrahydrofuran (5 ml). The solution is stirred at ambient temperature for 15 minutes and is then heated at 40° C. for 20 minutes. A solution of indole (6.75 mmol) in 40 ml of dry tetrahydrofuran is then added dropwise. After stirring for 1 hour at 40° C., the reaction mixture is cooled and then a solution of N-benzyloxymethyl-2,3-dibromomaleimide (3.38 mmol) in 40 ml of dry tetrahydrofuran is added dropwise. The reaction mixture is stirred for 15 hours and is then hydrolysed with saturated aqueous ammonium chloride solution. The organic product is extracted with ethyl acetate, and the organic phases are then combined, dried over magnesium sulphate and filtered. After evaporating off the solvent and purifng the residue by chromatography on silica gel (cyclohexane/ethyl acetate: 4/1), the expected product is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001906B2
Source datasetuspto-grants-2006_02
ORD IDord-d4f910cff7604c6c9ed03c88161f5350
Source noteuspto-grants-2006_02