HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060766Generated: October 27, 2026
Hydrochloric Acid → 3-(4-Methyl-indan-1-ylidene)-1,3-dihydroindol-2-one
https://huagongshe.com/reaction/1060766
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Oxindole | HCID 321710 | — |
| Reactant | 4-Methyl-1-indanone | HCID 4418431 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(4-Methyl-indan-1-ylidene)-1,3-dihydroindol-2-one | HCID 57014749 | 44.8% |
Reaction Steps
A mixture of 0.5 g 4-methyl-1-indanone, 1.37 g oxindole and 3 ml piperidine in 5 ml dimethylforamide was heated in a sealed tube at 130° C. for 3 days to yield a reddish-black suspension. The mixture was added to 1N hydrochloric acid solution and extracted with ethyl acetate. The organic layer was washed with brine dried over magnesium sulfate and concentrated. The resulting solid was precipitated from ethyl acetate/hexanes (2×) followed by methylene chloride/hexanes to afford 400 mg of 3-(4-methyl-indan-1-ylidene)-1,3-dihydroindol-2-one as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06525072B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-e4d260b575264bc6800198bd38fc86b3 |
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| Source note | uspto-grants-2003_02 |
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