HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-(Trifluoroacetylamino)-2,3-dihydrobenzofuran → 2,3-Dihydro-1-benzofuran-7-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-(Trifluoroacetylamino)-2,3-dihydrobenzofuran | HCID 21463492 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2,3-Dihydro-1-benzofuran-7-amine | HCID 12805950 | 96.2% |
Reaction Steps
A solution of 7-(trifluoroacetylamino)-2,3-dihydrobenzofuran (D2) (1.6 g) in methanol (30 ml) and 10% NaOH (3 ml) was heated to reflux for 24h. The mixture was evaporated under reduced pressure and partitioned between ethyl acetate and water. The organic phase was dried (Na2SO4) and the solvent evaporated under reduced pressure to give the title compound (900 mg, 96%) as a pale orange oil, which crystallised on standing.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05700818 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-8a7f6292877d4ba6b73be4be91a8a92f |
| Source note | uspto-grants-1997_12 |