HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → N-(2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluoroacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Aminoindane | HCID 76310 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(2,3-dihydro-1H-inden-2-yl)-2,2,2-trifluoroacetamide | HCID 10307996 | 82% |
Reaction Steps
Under N2 at −75° C., trifluoroacetic acid was added to a stirring solution of 2,3-dihydro-1H-inden-2-amine (HCl salt, 8.0 g, 47.2 mmol), Et3N (14.9 ml, 106.7 mmol) and THF (160 ml). After the solution was allowed to warm up to rt, it was partitioned between H2O and DCM. The organic layer was dried over MgSO4 and evaporated in vacuo. The residue was triturated with hexanes:Et2O (1:1) to obtain the product as a white solid (8.9 g, 82% yield). 1H-NMR (400 MHz, CDCl3) δ 7.28-7.20 (m, 4H), 6.50 (s, 1H), 4.81-4.74 (m, 1H), 3.38 (dd, J=16.4, 7.1 Hz, 2H), 2.89 (dd, J=16.3, 4.2 Hz, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07605174B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-8dccd7b66b49433fb5f2519728ddc272 |
| Source note | uspto-grants-2009_10 |