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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | N-[1-(4-bromophenyl)ethyl]acetamide | HCID 2854373 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[1-(4-iodophenyl)ethyl]acetamide | HCID 66634769 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08530460B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-9522183961e34526b56b95da231a4cb1 |
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| Source note | uspto-grants-2013_09 |
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