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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | 6-Methoxy-1-methyl-3,4-dihydroquinolin-2(1H)-one | HCID 10797787 | — |
| Catalyst | Silver trifluoroacetate | HCID 76299 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Iodo-6-methoxy-1-methyl-3,4-dihydro-1h-quinolin-2-one | HCID 21931742 | 48% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07119207B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-97e804b032474ed085e9864e322db833 |
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| Source note | uspto-grants-2006_10 |
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