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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009894Generated: October 26, 2026

Benzaldehyde → tert-butyl (3aR*,4S*,9bR)-4-phenyl-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline-1-carboxylate

https://huagongshe.com/reaction/1009894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantAnilineHCID 6115—
ReactantDysprosium tris(trifluoromethanesulfonate)HCID 9938788—
Reactanttert-Butyl 2,3-dihydro-1H-pyrrole-1-carboxylateHCID 10844857—
SolventAcetonitrileHCID 6342—
Producttert-butyl (3aR*,4S*,9bR)-4-phenyl-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline-1-carboxylateHCID 5784724031%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973163B2
Source datasetuspto-grants-2011_07
ORD IDord-658baf067233470cb3a9d62087ac74e3
Source noteuspto-grants-2011_07