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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516222Generated: October 30, 2026

Ethanol → HCID 58495251, compound

https://huagongshe.com/reaction/516222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 58495308HCID 58495308—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58495251HCID 58495251118%

Reaction Steps

To a solution of 1.772 g of t-butyl 11-chloro-2-oxo-1,2,3,4,6,7,9,10-octahydro-8H-azepino[4,5-g]quinoline-8-carboxylate in 10 ml of THF was added 10.1 ml of a 1 M solution of a borane-THF complex in THF under ice-cooling, followed by elevating to room temperature and stirring for 3 hours. To the reaction mixture was added dropwise 10 ml of EtOH, and subsequently 10 ml of a 1 M aqueous sodium hydroxide solution was added dropwise thereto, followed by stirring. The mixed solution was diluted with water, followed by extraction with EtOAc. The organic layer was dried over anhydrous sodium sulfate and then filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel chromatography (elution solvent: HEX-EtOAc) to obtain 2.007 g of t-butyl 11-chloro-1,2,3,4,6,7,9,10-octahydro-8H-azepino[4,5-g]quinoline-8-carboxylate as a colorless viscous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108977B2
Source datasetuspto-grants-2015_08
ORD IDord-f5df99eafda04497b7fe274b799235bf
Source noteuspto-grants-2015_08