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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041720Generated: October 25, 2026

Butanal → [(cis)-6-Bromo-2-propyl-1,2,3,4-tetrahydro-4-quinolinyl]formamide

https://huagongshe.com/reaction/2041720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButanalHCID 261—
Reactant4-BromoanilineHCID 7807—
ReactantN-VinylformamideHCID 83191—
ReactantHCID 178418385HCID 178418385—
Catalystp-Toluenesulfonic acid monohydrateHCID 521998—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product[(cis)-6-Bromo-2-propyl-1,2,3,4-tetrahydro-4-quinolinyl]formamideHCID 8666944829.9%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 1H-1,2,3-benzotriazole (3.46 g, 29.1 mmol) in toluene (38 mL) was added 4-bromoaniline (5.09 g, 29.1 mmol) in toluene (4.7 mL) and the reaction mixture was bubbled with Argon gas then cooled to 0° C. Butanal (2.88 mL, 32 mmol) in toluene (4.7 mL) was added dropwise and the resulting mixture was allowed to warm to room temperature and stirred for 16 h before being treated with ethenylformamide (2.03 mL, 29.1 mmol), 4-methylbenzenesulfonic acid monohydrate (55.3 mg, 0.29 mmol). The resulting mixture was stirred at 72° C. for 3 h then cooled to room temperature and diluted with AcOEt (50 mL). The organic phase was washed with a 1M NaOH aqueous solution (20 mL), water (50 mL) then brine (50 mL), dried over MgSO4 and concentrated in vacuovacuo. The residue was recrystallised from petroleum/Et2O (1:10, 3×30 mL) to give [(cis)-6-bromo-2-propyl-1,2,3,4-tetrahydro-4-quinolinyl]formamide (2.59 g, 29%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580957B2
Source datasetuspto-grants-2013_11
ORD IDord-25262e3daff04a399fad220f7be8036c
Source noteuspto-grants-2013_11