Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 550254Generated: October 26, 2026

Aniline → (3aR,4S,9bR)-1-tert-butyl 4-ethyl 3,3a,4,5-tetrahydro-1H-pyrrolo[3,2-c]quinoline-1,4(2H,9bH)-dicarboxylate

https://huagongshe.com/reaction/550254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantEthyl oxoacetateHCID 70211—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-Butyl 2,3-dihydro-1H-pyrrole-1-carboxylateHCID 10844857—
CatalystScandium(III) triflateHCID 2734571—
SolventTolueneHCID 1140—
Product(3aR,4S,9bR)-1-tert-butyl 4-ethyl 3,3a,4,5-tetrahydro-1H-pyrrolo[3,2-c]quinoline-1,4(2H,9bH)-dicarboxylateHCID 5784707246.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of ethyl glyoxylate (50% toluene solution, 13.76 g, 67.4 mmol) and aniline (5.6 ml, 61.3 mmol) in toluene (250 ml) was added magnesium sulfate (3.95 g, 32.85 mmol), and the mixture was stirred at 0° C. for 30 min. A solution of tert-butyl 2,3-dihydro-1H-pyrrole-1-carboxylate (10.37 g, 61.3 mmol) in toluene (50 ml) and scandium triflate (1.47 g, 3.0 mmol) were added at 0° C., and the mixture was stirred at room temperature for 16 hrs. Saturated aqueous sodium hydrogen carbonate solution was added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried (over anhydrous MgSO4), and the solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography and eluted with hexane-ethyl acetate (4:1-2:1, v/v). The title compound (3aR*,4R*,9bR*) (9.83 g, 46%) was obtained as an oil from the first eluted fraction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943770B2
Source datasetuspto-grants-2011_05
ORD IDord-14540daac3304939bd48c1a24422a41e
Source noteuspto-grants-2011_05