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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801285Generated: October 30, 2026

Isobutyraldehyde → Methyl 4-hydroxy-3,3-dimethyl-2-(4-nitrophenyl)-1,2,3,4-tetrahydroquinoline-6-carboxylate

https://huagongshe.com/reaction/1801285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyraldehydeHCID 6561—
ReactantHCID 178498134HCID 178498134—
CatalystYttrium trifluoromethanesulfonateHCID 2733939—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-hydroxy-3,3-dimethyl-2-(4-nitrophenyl)-1,2,3,4-tetrahydroquinoline-6-carboxylateHCID 6744302620%

Reaction Steps

To a solution of (E)-methyl 4-(4-nitrobenzylideneamino)benzoate (284 mg 1 mmol) and yttrium(III) trifluoromethanesulfonate (62 mg, 0.1 mmol) in tetrahydrofuran (5 mL) was added isobutyraldehyde (72 mg, 1.5 mmol). The resultant mixture was stirred at room temperature for 16 h. Thin layer chromatography showed the starting material was completely consumed. The reaction mixture was quenched with water and separated. The aqueous solution was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. Solvent was removed in vacuo to give the crude product, which was purified by column chromatography (petroleum ether/ethyl acetate=3:1) to afford 70 mg of methyl 4-hydroxy-3,3-dimethyl-2-(4-nitrophenyl)-1,2,3,4-tetrahydroquinoline-6-carboxylate as a yellow solid. Yield: 20%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08344137B2
Source datasetuspto-grants-2013_01
ORD IDord-1f2ae1c9a0d443a3b3ed7f64cf9c4c43
Source noteuspto-grants-2013_01