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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1417486Generated: October 31, 2026

Diethyl Ether → 1-(1-Benzyl-1H-indol-4-yl)ethan-1-one

https://huagongshe.com/reaction/1417486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-Benzyl-1H-indole-4-carbonitrileHCID 29012041—
ReactantHCID 178418373HCID 178418373—
SolventTetrahydrofuranHCID 8028—
Product1-(1-Benzyl-1H-indol-4-yl)ethan-1-oneHCID 15917670—

Reaction Steps

3.3 ml of a 2M solution of methylmagnesium iodide in diethyl ether was added to a mixture of 1.00 g of 1-benzyl-4-cyanoindole (prepared as described in Example 88) in 50 ml of tetrahydrofuran, with ice-cooling, and the reaction mixture was stirred for 1 hour. After this time, a saturated aqueous solution of ammonium chloride was added to the reaction mixture. The aqueous layer was extracted with diethyl ether, and the resulting organic fraction was washed with water, dried over anhydrous magnesium sulfate and concentrated by evaporation under reduced pressure. The resulting residue was purified by silica gel column chromatography, using 50 g of silica gel and a 4:1 v/v mixture of hexane and ethyl acetate as the eluent, to yield 1.00 g of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05877199
Source datasetuspto-grants-1999_03
ORD IDord-a00412a7d9f141e2ab3ffb4f0a258e9c
Source noteuspto-grants-1999_03