Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Indoline | HCID 10328 | — |
| Reactant | HCID 53411290 | HCID 53411290 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 4448611 | HCID 4448611 | 86.1% |
Reaction Steps
Triethylamine (9.2 ml) was added at room temperature to a solution of indoline (20 g) in DCM (200 ml) and the mixture was cooled till 5° C. A solution of m-chloro-cinnamoyl chloride (40 g) in DCM (100 ml) was added dropwise and the mixture was stirred at room temperature for 48 hours. Water was added, the organic layer was decanted, washed with water, dried, filtered off and evaporated. The residue was purified by column chromatography over silica gel (eluent: cyclohexane/ethyl acetate 90/10), yielding 41 g (73%) of 1-[3-(3-chlorophenyl)-1-oxo-2-propenyl]-2,3-dihydro-1H-indole (interm. 37).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06187786B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-28287d05088a435da52add8df74eaf92 |
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| Source note | uspto-grants-2001_02 |
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