HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856905Generated: October 31, 2026
Iodine → N-[2-(3-Iodo-7-methoxy-1-naphthyl)ethyl]acetamide
https://huagongshe.com/reaction/1856905
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | Agomelatine | HCID 82148 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[2-(3-Iodo-7-methoxy-1-naphthyl)ethyl]acetamide | HCID 22133330 | — |
Reaction Steps
A solution is formed by adding 46.25 ml of glacial acetic acid and 1.25 ml of concentrated sulphuric acid to 2.5 ml of water. 2.5 g of N-[2-(7-methoxy-1-naphthyl)ethyl]acetamide (10.31 mmol) are dissolved in 30 ml of that solution. 2.09 g of iodine (8.25 mmol) and 0.91 g of HIO3 (5.16 mmol) are then added to the reaction mixture, causing a grey precipitate to appear in a solution that has turned red. The reaction mixture is heated for 15 hours at 65° C., 5.14 ml of concentrated hydriodic acid (13.41 mmol) are added and heating is continued for 2 hours. The suspension is then poured into 200 ml of water and the precipitate that forms is filtered off. The precipitate is dissolved in ethyl acetate and washed with 1M NaHCO3, the organic phase is then concentrated, and purified by chromatography on silica gel, using a dichloromethane/methanol mixture, 99.5/0.5, as eluant, to yield the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06143789 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-1a4be8483b224d8fbe142c3b128bf815 |
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| Source note | uspto-grants-2000_11 |
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