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Water → Ethyl 6-hydroxy-5-iodonicotinate

HRID 1690193
ノート
印刷プレビュー

反応式

HRID 1690193 の反応式
[OH:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][N:3]=1.[I-:13].O>N1C=CC=CC=1>[OH:1][C:2]1[C:12]([I:13])=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][N: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 3

HCID 962WaterHCID 30165Iodide IonHCID 178469094HCID 178469094、化合物

生成物 1

HCID 178469850Ethyl 6-hydroxy-5-iodonicotinate収率 83%

試薬・触媒・溶媒 1

HCID 1049Pyridine溶媒

反応条件

温度
60 °C

実験手順

Ethyl 6-hydroxynicotinate (2.0 g, 12.0 mmol) was dissolved in pyridine (60 mL), which was then added with iodide (6.07 g, 23.9 mmol) and stirred at 60° C. overnight. The reaction solution was then added with water at room temperature and extracted with ethyl acetate. Subsequently, the organic layer was washed with a saturated aqueous solution of sodium sulfite and brine, and dried over sodium sulfate. The obtained residue was purified using column chromatography (chloroform/methanol) and concentrated in vacuo. Ethyl 6-hydroxy-5-iodonicotinate (2.9 g, yield 83%) was obtained as a yellow oil.

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート

後処理

  1. extractionextracted with ethyl acetate
  2. washSubsequently, the organic layer was washed with a saturated aqueous solution of sodium sulfite and brine
  3. dry with materialdried over sodium sulfate
  4. customThe obtained residue was purified
  5. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-ca1f2f17b944479d9b6fe4e4f2acb72e
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08153634B2

反応ノート

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