Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantHydrogen iodideHCID 24841—
ReactantAgomelatineHCID 82148—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductN-[2-(3-Iodo-7-methoxy-1-naphthyl)ethyl]acetamideHCID 22133330—

Reaction Conditions

Temperature65 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143789
Source datasetuspto-grants-2000_11
ORD IDord-1a4be8483b224d8fbe142c3b128bf815
Source noteuspto-grants-2000_11