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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097434Generated: November 1, 2026

Sulfuric Acid → 5-Bromo-3,4-dihydroquinolin-2(1H)-one

https://huagongshe.com/reaction/1097434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AzideHCID 33557—
Reactant1-Indanone, 4-bromo-HCID 98713—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product5-Bromo-3,4-dihydroquinolin-2(1H)-oneHCID 53249793—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred mixture of sodium azide (862 mg, 13.3 mmol) in H2O (1.7 mL) and CHCl3 (6.5 mL) was added conc. H2SO4 (0.23 mL, 4.14 mmol). The reaction mixture was stirred vigorously at 0° C. for 2.5 h. The CHCl3 layer was separated, dried over Na2SO4, and added to a solution of 4-bromo-1-indanone (1.12 g, 5.31 mmol) in CHCl3 (20 mL). To this mixture was added conc. H2SO4 (1.75 mL, 31.5 mmol) dropwise over 10 min. The reaction mixture was heated at 45 C for 1 h then poured into ice-water, neutralized with 20% aqueous NaOH, and extracted with CH2Cl2 (100 mL). The organic extract was dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by silica gel chromatography, eluting with a gradient of CH2Cl2:EtOAc—100:0 to 80:20, to give the title compound. MS: m/z=226 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143266B2
Source datasetuspto-grants-2012_03
ORD IDord-81a89f9404ff45b48f5d77a4945df4a4
Source noteuspto-grants-2012_03