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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550253Generated: October 25, 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/550253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantAnilineHCID 6115—
ReactantDysprosium(III) trifluoromethanesulfonateHCID 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 numberUS07943770B2
Source datasetuspto-grants-2011_05
ORD IDord-e0825e07e429430a8e487a2c3b205a42
Source noteuspto-grants-2011_05