Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 21071407 | HCID 21071407 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 21071615 | HCID 21071615 | — |
Reaction Steps
Dissolve 2-(2-(7-fluoro-1H-indol-3-yl)ethyl)isoindole-1,3-dione in 25 mL of THF. Add ethanolamine (63.4 g, 62.65 mL, 1038 mmol, 100 eq.) with vigorous stirring and heat to 70° C. After 1.5 hours, cool to room temperature. After 18 hours, pour reaction mixture into of water (250 mL) containing of 5N NaOH (3 mL) and extract with Et2O (2×200 mL). Combine the organic layers and wash with 0.1 N NaOH. Collect the organic layer, dry over MgSO4, filter, and remove the solvent in vacuo to give the title compound as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044090B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-06afa83982ae4b2c8411e6c69842a6a4 |
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| Source note | uspto-grants-2011_10 |
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