HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → tert-Butyl (3aR*,4S*,9bR)-3a-methyl-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 | N-Boc-3-methyldihydropyrrole | HCID 67150753 | — |
| Catalyst | Dysprosium tris(trifluoromethanesulfonate) | HCID 9938788 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | tert-Butyl (3aR*,4S*,9bR)-3a-methyl-4-phenyl-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline-1-carboxylate | HCID 57847178 | 53.5% |
Reaction Steps
To a mixture of benzaldehyde (425 mg, 4.0 mmol), aniline (372 mg, 4.0 mmol) and acetonitrile (8 ml) were added N-Boc-3-methyldihydropyrrole (732 mg, 4.0 mmol) and Dy(OTf)3 (122 mg, 0.19 mmol) under ice-cooling, and the mixture was stirred at the same temperature for 30 min., and at room temperature for 1 hr. 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 (over anhydrous MgSO4), and concentrated under reduced pressure. The residue was subjected to column chromatography using silica gel (30 g) and eluted with hexane-ethyl acetate (4:1, v/v) to give the title compound (780 mg, 53%) as an amorphous form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07943770B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-70473beb08804f3881e0577c0d98347c |
| Source note | uspto-grants-2011_05 |