Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Oxindole | HCID 321710 | — |
| Reactant | 5-Bromo-1-indanone | HCID 520695 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57126539 | HCID 57126539 | 11.2% |
Reaction Steps
A reaction mixture of 0.422 g 5-bromoindanone, 1.3 g oxindole and 0.9 ml piperidine in 3 ml of dimethylforamide was heated in a sealed tube at 110° C. overnight. The reaction mixture was poured into ice water and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated. The black residue was chromatographed on a silica gel column, eluting with ethyl acetate and hexane to give 73.0 mg of 3-(5-bromoindan-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 | US06642251B1 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-c53a29bae8174d12926ea1b653e77928 |
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| Source note | uspto-grants-2003_11 |
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