HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1446586Generated: October 25, 2026
Triethylamine → 1-(1H-indol-3-yl)ethanone oxime
https://huagongshe.com/reaction/1446586
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Acetylindole | HCID 12802 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(1H-indol-3-yl)ethanone oxime | HCID 3014124 | 96.9% |
Reaction Steps
Triethylamine (3.93 mL) was added to a solution of 3-acetylindole (500 mg) and hydroxylamine hydrochloride (981 mg) in ethanol (20 mL), and the reaction solution was heated to reflux at 90° C. for 14 hours. The reaction solution was allowed to be cooled to room temperature, the solvent was concentrated under reduced pressure, and ethyl acetate and water were added to the resulting residue and the organic layer was partitioned. The resulting organic layer was washed with brine, and then dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel chromatography (elution solvent:ethyl acetate) to obtain 0.53 g of the title compound. The physical properties of the compound are as follows.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07667041B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-2e77dc2aac9748d29cface87b3c2aad8 |
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| Source note | uspto-grants-2010_02 |
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