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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853007Generated: October 30, 2026

Butylamine → Butyl (4-chloroquinolin-6-ylmethylene)-amine

https://huagongshe.com/reaction/853007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButylamineHCID 8007—
ReactantTetrahydrofuranHCID 8028—
Reactant4-Chloroquinoline-6-carbaldehydeHCID 53417226—
SolventEthyl AcetateHCID 8857—
ProductButyl (4-chloroquinolin-6-ylmethylene)-amineHCID 58615380100%

Reaction Steps

To a suspension of 4-chloro-quinoline-6-carbaldehyde (3.59 g, 18.73 mmol) in heptanes (36 mL) was added n-butylamine(1.51 g, 20.60 mmol, 1.1 equiv.) at room temperature. The reaction mixture was stirred for 5 h at room temperature by this time all solids were dissolved and gave a light brown solution containing a little oily stuff on the wall of flask. Then, 4 mL of THF was added and the clear solution was stirred for another 15 h. This solution was diluted with ethyl acetate (50 mL) and washed with brine solution and dried over anhydrous magnesium sulfate. After filtration of the drying agent, the solvents were removed under the vacuum and the remaining residue was dried under high vacuum to afford 4.62 g (˜100% yield) of butyl (4-chloro-quinolin-6-ylmethylene)-amine as a brown oil which was used directly for the next substitution reaction. LRMS(+) m/e calcd for C14H15ClN2 (M+H)+247.7, found 247.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253285B2
Source datasetuspto-grants-2007_08
ORD IDord-5668e3213f134148a6ab76af18e99724
Source noteuspto-grants-2007_08