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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735724Generated: October 26, 2026

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

https://huagongshe.com/reaction/735724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantAnilineHCID 6115—
ReactantN-Boc-3-methyldihydropyrroleHCID 67150753—
CatalystDysprosium tris(trifluoromethanesulfonate)HCID 9938788—
SolventAcetonitrileHCID 6342—
Producttert-Butyl (3aR*,4S*,9bR)-3a-methyl-4-phenyl-2,3,3a,4,5,9b-hexahydro-1H-pyrrolo[3,2-c]quinoline-1-carboxylateHCID 5784717853.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592453B2
Source datasetuspto-grants-2009_09
ORD IDord-0704054460d040eda588b273d75ebfb3
Source noteuspto-grants-2009_09