HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → tert-butyl (3aR*,4S*,9bR)-4-phenyl-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Dysprosium(III) trifluoromethanesulfonate | HCID 9938788 | — |
| Reactant | tert-Butyl 2,3-dihydro-1H-pyrrole-1-carboxylate | HCID 10844857 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | tert-butyl (3aR*,4S*,9bR)-4-phenyl-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline-1-carboxylate | HCID 57847240 | 31% |
Reaction Steps
Benzaldehyde (2.92 g, 28 mmol), aniline (2.56 g, 28 mmol), tert-butyl 2,3-dihydro-1H-pyrrole-1-carboxylate (3.4 g, 25 mmol) and Dy(OTf)3 (0.61 g, 1.38 mmol) were stirred in acetonitrile (50 ml) at room temperature for 2 hrs. The reaction mixture was concentrated under reduced pressure, water was added and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried (anhydrous MgSO4), and the solvent was evaporated under reduced pressure. The residue was subjected to column chromatography using silica gel (150 g), and eluted with hexane-ethyl acetate (4:1, v/v). The title compound (3aR*,4R*,9bR*) (2.7 g, 31%) was obtained as an amorphous form from the first eluted fraction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943770B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-e0825e07e429430a8e487a2c3b205a42 |
| Source note | uspto-grants-2011_05 |