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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 735751Generated: October 27, 2026

Benzaldehyde → tert-butyl (4aS*,5R*,10bS*)-5-phenyl-3,4,4a,5,6,10b-hexahydrobenzo[h]-1,6-naphthyridine-1(2H)-carboxylate

https://huagongshe.com/reaction/735751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantAnilineHCID 6115—
ReactantDysprosium tris(trifluoromethanesulfonate)HCID 9938788—
ReactantTert-butyl 1,2,3,4-tetrahydropyridine-1-carboxylateHCID 10465102—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Producttert-butyl (4aS*,5R*,10bS*)-5-phenyl-3,4,4a,5,6,10b-hexahydrobenzo[h]-1,6-naphthyridine-1(2H)-carboxylateHCID 671507206%

Reaction Steps

Benzaldehyde (531 mg, 5 mmol) was dissolved in acetonitrile (15 ml), aniline (466 mg, 5 mmol) was added at 0° C., and the mixture was stirred at the same temperature for 1 hr. tert-Butyl 3,4-dihydropyridine-1(2H)-carboxylate (917 mg, 5 mmol) and Dy(OTf)3 (153 mg, 0.25 mmol) were added at 0° C., and the mixture was further stirred for 1.5 hrs. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with 6% aqueous sodium hydrogen carbonate solution and saturated brine and dried (over anhydrous MgSO4), and the solvent was evaporated under reduced pressure. The residue was subjected to column chromatography using silica gel (100 g), and eluted with hexane-ethyl acetate (19:1-6:1, v/v). The title compound (4aR*,5R*,10bR*) (109 mg, 6%) was obtained as a colorless amorphous form from the first eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592453B2
Source datasetuspto-grants-2009_09
ORD IDord-9804ea1cf1d14d20a6fdaf9518affbdf
Source noteuspto-grants-2009_09