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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-Benzyl-1H-indole-4-carbonitrile | HCID 29012041 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-(1-Benzyl-1H-indol-4-yl)ethan-1-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05877199 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-a00412a7d9f141e2ab3ffb4f0a258e9c |
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| Source note | uspto-grants-1999_03 |
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