HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(2,3-Dihydro-1H-inden-1-yl)butanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | (+-)-1-Aminoindan | HCID 123445 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | N-(2,3-Dihydro-1H-inden-1-yl)butanamide | HCID 18627825 | 58% |
Reaction Steps
A solution of butyryl chloride (5.33 g, 50 mmole) in anh. DME (60 ml) was added slowly to a stirred and ice-cooled solution of 1-aminoindan (6.66 g, 50 mmole) and Et3N (10.0 g, 100 mmole) in anh. DME (75 ml), and the mixture stirred at ambient temperature for 24 hr. After removal of volatiles under reduced pressure, the residue was taken up in 1:1 water/EtOAc mixture (300 ml). The organic layer was separated, dried on Na2SO4 and evaporated to dryness. The crude product was crystallized from EtOAc, to give 5.9 g (58%) of the title compound as a white solid, m.p.: 84°-5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06271263B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-12e7a61e267b453890c4fbd32269b18a |
| Source note | uspto-grants-2001_08 |