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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396870Generated: October 30, 2026

Benzyl chloroformate → HCID 18762415, compound

https://huagongshe.com/reaction/396870

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium HydroxideHCID 14798—
Reactant1,4-DioxaneHCID 31275—
Reactant3-Aminoquinolin-2(1H)-oneHCID 10103424—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 18762415HCID 1876241535.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution containing 0.5 g (3.10 mmol) of 3-amino-quinoline-2-(1H)-one described by Anderson, et. al. (J. Heterocyclic Chem., 30:1533 (1993)) in 40 mL, of dioxane under a nitrogen atmosphere was added 0.14 g (3.4 mmol) of sodium hydroxide in 14 ml, of water. The reaction mixture was cooled to 0° C., followed by the addition of 0.50 mL (3.4 mmol) of benzylchloroformate. The pH of the reaction was maintained above 8.0 with additional 1 N sodium hydroxide. The reaction was allowed to warm to room temperature and stirred for 2 hours. The reaction was diluted with methylene chloride and washed with water. The organic phase was dried over magnesium sulfate. Filtration, removal of solvent under reduced pressure and column chromatography of the residue on silica gel with 2% methanol/dichloromethane afforded 0.32 g (35%) of product as a white solid. FAB MS [M+H] m/z; Calcd: 295, Found: 295

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608175B2
Source datasetuspto-grants-2003_08
ORD IDord-5dcd60d21e024e2eab044b09e5f4bda7
Source noteuspto-grants-2003_08