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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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2-Bromopropane → HCID 86654668, 화합물

HRID 880449
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HRID 880449 반응식
[H-].[Na+].[I:3][C:4]1[CH:5]=[C:6]([CH:9]=[O:10])[NH:7][CH:8]=1.Br[CH:12]([CH3:14])[CH3:13]>CN(C)C=O>[I:3][C:4]1[CH:5]=[C:6]([CH:9]=[O:10])[N:7]([CH:12]([CH3:14])[CH3:13])[CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 63582-BromopropaneHCID 24758Sodium hydrideHCID 46719534-iodo-1H-pyrrole-2-carbaldehyde

생성물 1

HCID 86654668HCID 86654668, 화합물수율 43.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

Sodium hydride (860 mg, 55% in mineral oil, 19.7 mmol) was added to a solution of 4-iodo-pyrrole-2-carbaldehyde (3.0 g, 13.2 mmol) in dry dimethylformamide at ambient temperature under a nitrogen atmosphere. After stirring for 15 min 2-bromopropane (3.87 mL, 40.9 mmol) was added and the reaction mixture heated at reflux for 16 h. The mixture was allowed to cool to ambient temperature, quenched with water and extracted with diethyl ether. The combined organic layers were washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give a crude residue. Purification by column chromatography over silica gel (60-120 mesh) using 2% ethyl acetate in petroleum ether afforded 4-iodo-1-isopropyl-pyrrole-2-carbaldehyde (1.5 g, 43%) as a brown liquid.

후처리

  1. additionwas added
  2. temperaturethe reaction mixture heated
  3. temperatureat reflux for 16 h
  4. customquenched with water
  5. extractionextracted with diethyl ether
  6. washThe combined organic layers were washed with water, brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. concentrationconcentrated in vacuo
  9. customto give a crude residue
  10. customPurification by column chromatography over silica gel (60-120 mesh)

출처 및 근거

ORD 기록
ord-f4514892561e4adb88c0b1fde885f87c
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08993574B2

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