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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874803Generated: October 25, 2026

1-Methyl-1,4-cyclohexadiene → (R)-5-(2-Amino-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one hydrochloride

https://huagongshe.com/reaction/874803

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-1,4-cyclohexadieneHCID 78006—
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Reactant(R)-5-(2-Azido-1-((tert-butyldimethylsilyl)oxy)ethyl)-8-(benzyloxy)quinolin-2(1H)-oneHCID 58505233—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(R)-5-(2-Amino-1-hydroxyethyl)-8-hydroxyquinolin-2(1H)-one hydrochlorideHCID 7109324164.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of (R)-5-(2-azido-1-((tert-butyldimethylsilyl)oxy)ethyl)-8-(benzyloxy)quinolin-2(1H)-one (4.50 g, 10.0 mmol) in ethanol (50 mL) was added 10% palladium on charcoal (4.50 g) followed by 1-methyl-1,4-cyclohexadiene (11.0 mL, 97.9 mmol). The reaction was warmed to 60° C. (CARE—POSSIBLE EXOTHERM) and then stirred at 60° C. for 2 hours. The reaction mixture was allowed to cool and filtered through a pad of celite. The filter cake was washed with further ethanol and the filtrate was evaporated at reduced pressure. The residue was evaporated from iso-propanol (×2) and dissolved in iso-propanol (30 mL). HCl-dioxane (4 M, 50 mL, 200 mmol) was added and the reaction mixture stirred at RT for 18 hours. The resultant suspension was filtered, the filter cake washed with ether and the solid dried under vacuum in the presence of P2O5 to afford the title compound (1.65 g, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980913B2
Source datasetuspto-grants-2015_03
ORD IDord-fc23fa6bd2ca4bf895a5a9e6ed3c2fa5
Source noteuspto-grants-2015_03