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

HRID 40559
ノート
印刷プレビュー

反応式

HRID 40559 の反応式
Br[C:2]1[CH:7]=[CH:6][C:5]([CH:8]([NH:10][C:11](=[O:13])[CH3:12])[CH3:9])=[CH:4][CH:3]=1.[Na+].[I-:15]>O1CCOCC1.[Cu]I>[I:15][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([NH:10][C:11](=[O:13])[CH3:12])[CH3:9])=[CH:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 5238Sodium IodideHCID 2854373N-[1-(4-bromophenyl)ethyl]acetamide

生成物 1

HCID 66634769N-[1-(4-iodophenyl)ethyl]acetamide

試薬・触媒・溶媒 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)触媒HCID 312751,4-Dioxane溶媒

反応条件

温度
120 °C

実験手順

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.

後処理

  1. temperatureto cool to r.t.
  2. customhalf of the solvent is removed in vacuo
  3. additionEtOAc and diluted aq. ammonia solution are added
  4. customthe layers are separated
  5. extractionThe aq. layer is once more extracted with EtOAc
  6. dry with materialdried with Na2SO4
  7. customthe solvent is removed in vacuo
  8. customThe crude product is triturated with diethylether
  9. customdried in vacuo

出典と根拠

ORDレコード
ord-9522183961e34526b56b95da231a4cb1
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08530460B2

反応ノート

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