Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | 113405-11-1 | HCID 2767551 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Benzofuranacetamide | HCID 17976493 | — |
Reaction Steps
Add 1,1′-carbonyldiimidazole (2.3 g, 14.2 mmol) to a solution of 2-(benzofur-4-yl)acetic acid (2.5 g, 14.2 mmol) in anhydrous tetrahydrofuran (12 mL) under nitrogen and stir at 20° C. for 4 hours. Bubble anhydrous ammonia through the solution, dilute with anhydrous tetrahydrofuran (10 mL) and stir at 20° C. for 18 hours. Concentrate under reduced pressure, wash the solid with aqueous sodium hydrogen sulfate, distilled water, and dry under vacuum to obtain the title compound as a pale yellow solid
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022065B2 |
|---|
| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-7e22d6b248994e10ae2ddd9cafec31b1 |
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| Source note | uspto-grants-2011_09 |
|---|