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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1244023Generated: October 30, 2026

Iodine → 7-Iodo-6-methoxy-1-methyl-3,4-dihydro-1h-quinolin-2-one

https://huagongshe.com/reaction/1244023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant6-Methoxy-1-methyl-3,4-dihydroquinolin-2(1H)-oneHCID 10797787—
CatalystSilver trifluoroacetateHCID 76299—
SolventDichloromethaneHCID 6344—
Product7-Iodo-6-methoxy-1-methyl-3,4-dihydro-1h-quinolin-2-oneHCID 2193174248%

Reaction Steps

Silver trifluoroacetate (2.32 g, 10.48 mmol) was added to a dry methylene chloride (100 ml) solution of 6-Methoxy-1-methyl-3,4-dihydro-1H-quinolin-2-one (1.0 g, 5.24 mmol) followed by the dropwise addition of methylene chloride (100 ml) solution of iodine (1.33 g, 10.48 mmol) over 15 minutes. The reaction mixture was stirred overnight and the precipitated silver iodide salts were filtered off. The filtrate was concentrated down to a residue which was chromatographed using 50% ethylacetate/hexane to yield the title compound (795 mg, 48% yield). 1H NMR (400 MHz, CDCl3) δ 2.57–2.61 (2H, m), 2.81–2.85 (2H, m), 3.27 (3H, s), 3.82 (3H, s), 6.62 (1H, s), 7.31 (1H, s). m/z (APCI+) 318 (M+1). HPLC (aqueous 200 Mm ammonium acetate buffer/acetonitrile gradient, 3.0 ml/min, Hewlett Packard ODS Hypersil 5 μM, 125×4 mm column), 4.959 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119207B2
Source datasetuspto-grants-2006_10
ORD IDord-97e804b032474ed085e9864e322db833
Source noteuspto-grants-2006_10