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Acetic Acid → HCID 86654669、化合物

HRID 880450
ノート
印刷プレビュー

反応式

HRID 880450 の反応式
[OH-].[K+].[I:3][C:4]1[CH:5]=[C:6]([CH:9]=[O:10])[NH:7][CH:8]=1.Br[CH2:12][CH2:13][OH:14].C(O)(=O)C>O1CCOCC1>[OH:14][CH2:13][CH2:12][N:7]1[CH:8]=[C:4]([I:3])[CH:5]=[C:6]1[CH:9]=[O:10]
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

6

反応物 4

HCID 176Acetic AcidHCID 108982-BromoethanolHCID 14797Potassium HydroxideHCID 46719534-iodo-1H-pyrrole-2-carbaldehyde

生成物 1

HCID 86654669HCID 86654669、化合物収率 50%

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

反応条件

温度
60 °C

実験手順

Potassium hydroxide (3.1 g, 54.3 mmol) was added to a stirred solution of 4-iodo-1H-pyrrole-2-carbaldehyde (4.0 g, 18.1 mmol) in dioxane (20 mL). 2-Bromo-ethanol (2.56 mL, 36.2 mmol) was added to the reaction mixture and heated at 60° C. for 16 h. The reaction mixture was cooled to room temperature and the pH was adjusted to ˜6 by the addition of acetic acid. The reaction mixture was then concentrated in vacuo to give a residue which was partitioned between water and ethyl acetate. The organic phase was washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give a residue which was purified by column chromatography over silica gel (100-200 mesh) using 10% ethyl acetate in petroleum ether as eluent to afford 1-(2-hydroxyethyl)-4-iodo-pyrrole-2-carbaldehyde (2.4 g, 50%) as a colourless solid.

後処理

  1. temperatureThe reaction mixture was cooled to room temperature
  2. concentrationThe reaction mixture was then concentrated in vacuo
  3. customto give a residue which
  4. customwas partitioned between water and ethyl acetate
  5. washThe organic phase was washed with water, brine
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated in vacuo
  8. customto give a residue which
  9. customwas purified by column chromatography over silica gel (100-200 mesh)

出典と根拠

ORDレコード
ord-915adc9b33144c15bcec9faf39cdf7b0
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08993574B2

反応ノート

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