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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555325Generated: October 26, 2026

Water → HCID 66988296, compound

https://huagongshe.com/reaction/555325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantHydrocarbostyrilHCID 64796—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
Reactanttert-Butyl (6-bromohexyl)carbamateHCID 16211353—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66988296HCID 66988296—

Reaction Steps

0.5M Potassium bis-(trimethylsilyl)-amide in toluene (10 ml) was added dropwise at −30° C. in an argon atmosphere to a stirred solution of 2-oxo-1,2,3,4-tetrahydroquinoline (735 mg) in tetrahydrofuran (50 ml). After further cooling to −50° C. a solution of N-(tert-butoxycarbonyl)-6-bromo-hexylamine (1.5 g) in tetrahydrofuran (10 ml) was added slowly. Subsequently the temperature was allowed to raise to room temperature followed by heating at 50-60° C. for 48 hours. Ice and water were added and the mixture was extracted twice with ethyl acetate. The organic phases were washed with saturated sodium chloride, dried and evaporated to leave a yellow oil which after purification by chromatography on silica gel with ethyl acetate/hexane (1:1) as eluent gave the desired compound as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053446B2
Source datasetuspto-grants-2011_11
ORD IDord-755de4918fee4d9aa5ce21b2aa2929dd
Source noteuspto-grants-2011_11