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Acetic Acid → HCID 86654669, 화합물

HRID 880450
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HRID 880450 반응식
[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]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

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

생성물 1

HCID 86654669HCID 86654669, 화합물수율 50%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

반응 조건

온도
60 °C

실험 절차

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.

후처리

  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)

출처 및 근거

ORD 기록
ord-915adc9b33144c15bcec9faf39cdf7b0
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08993574B2

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