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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40559Generated: October 27, 2026

Sodium Iodide → N-[1-(4-iodophenyl)ethyl]acetamide

https://huagongshe.com/reaction/40559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantN-[1-(4-bromophenyl)ethyl]acetamideHCID 2854373—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
ProductN-[1-(4-iodophenyl)ethyl]acetamideHCID 66634769—

Reaction Conditions

Temperature120 °C

Reaction Steps

To 8.70 g (35.9 mmol) N-(1-(4-bromophenyl)ethyl)acetamide (III.2) in 100 mL 1,4-dioxane are added 0.69 g (3.62 mmol) CuI, 0.97 mL (9.11 mmol) N,N″-dimethyl-ethylendiamine and 10.8 g (71.9 mmol) NaI. The reaction mixture is stirred at 120° C. for 3 d. The mixture is allowed to cool to r.t. and half of the solvent is removed in vacuo. EtOAc and diluted aq. ammonia solution are added and the layers are separated. The aq. layer is once more extracted with EtOAc. The organic layers are combined, dried with Na2SO4 and the solvent is removed in vacuo. The crude product is triturated with diethylether and dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530460B2
Source datasetuspto-grants-2013_09
ORD IDord-9522183961e34526b56b95da231a4cb1
Source noteuspto-grants-2013_09