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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14242Generated: October 23, 2026

Butyl bromide → Methyl 1-butyl-1,2,3,4-tetrahydroquinoline-7-carboxylate

https://huagongshe.com/en/reaction/14242

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl bromideHCID 8002—
ReactantCesium bicarbonateHCID 2734983—
ReactantMethyl 1,2,3,4-tetrahydroquinoline-7-carboxylateHCID 16244389—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductMethyl 1-butyl-1,2,3,4-tetrahydroquinoline-7-carboxylateHCID 2108613167.1%

Reaction Steps

To a stirred solution of methyl 1,2,3,4-tetrahydroquinoline-7-carboxylate (180 mg, 0.94 mmol) and cesium bicarbonate (1.5 g, 4.7 mmol) in THF (2 mL) was added n-butyl bromide (1.0 mL, 9.4 mmol), and the reaction mixture was heated at reflux for 48 h. The reaction mixture was cooled to room temperature, and diluted with EtOAc. The organic layer was washed with water, and brine, dried (magnesium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:3 ethyl acetate/hexanes) afforded methyl 1-butyl-1,2,3,4-tetrahydroquinoline-7-carboxylate (156 mg): ESI MS m/z 248 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727997B2
Source datasetuspto-grants-2010_06
ORD IDord-3aaa66ee44c24706a33c8f1585534b8e
Source noteuspto-grants-2010_06