Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39217Generated: October 25, 2026

Triethylamine → 4-Bromo-1-(octahydroquinolin-1-yl)butan-1-one

https://huagongshe.com/reaction/39217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantDecahydroquinolineHCID 92911—
Reactant5-Bromovaleryl chlorideHCID 521173—
Product4-Bromo-1-(octahydroquinolin-1-yl)butan-1-oneHCID 66794644—

Reaction Steps

1.37 mL (9.9 mmol) of Et3N and 0.5 mL (4.5 mmol) of 5-bromovaleric acid chloride are added to a solution of 1 mL (4.0 mmol) of the decahydroquinoline in AcOEt. The resulting solution is kept under stirring for 18 h at rt. The solution is then washed with water, and the water re-extracted twice with AcOEt. The pooled organic phases are sequentially washed with 5% solution of NaHCO3, 1N HCl and saturated ammonium chloride solution. Finally the organic phase is dried over anhydrous Na2SO4, it is filtered and the solvent is evaporated under reduced pressure. 1.2 g of a yellow oil, which was used without subsequent purification, are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524894B2
Source datasetuspto-grants-2013_09
ORD IDord-4385fe3b05a5409db891b352d1f7b58c
Source noteuspto-grants-2013_09