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Imidazole → 1-Isopropyl-1H-imidazole-2-carbaldehyde

HRID 899837
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HRID 899837 반응식
[NH:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[Li][CH2:7][CH2:8][CH2:9]C.CN([CH:14]=[O:15])C>C1COCC1>[CH:8]([N:1]1[CH:5]=[CH:4][N:3]=[C:2]1[CH:14]=[O:15])([CH3:9])[CH3:7]
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참가 물질

5

반응물 3

HCID 795ImidazoleHCID 6228DimethylformamideHCID 178418339Butyllithium

생성물 1

HCID 100575681-Isopropyl-1H-imidazole-2-carbaldehyde수율 65.5%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
0 °C

실험 절차

A solution of the imidazole (890 mg, 8.08 mmol) in THF (10 mL) under nitrogen was cooled to −78° C. and n-BuLi (2.5M in hexanes, 4.5 mL, 11.3 mmol) was added. The bright yellow solution was stirred at 0° C. for 25 minutes, then DMF (1.5 mL, 19 mmol) was added. The reaction was stirred at room temperature for one hour, then was quenched by the addition of saturated aqueous NH4Cl (10 mL). The layers were separated and the aqueous solution was extracted with EtAOc (10 mL×2). The combined organic solution was dried (Na2SO4), filtered and concentrated under reduced pressure. Purification by flash column chromatography on silica (hexane/EtOAc, 1:1) gave the aldehyde as a pale yellow solid (731 mg, 5.29 mmol, 65%). 1H NMR (CDCl3) δ 1.46 (d, 6H, J=6.6 Hz), 5.46 (septet, 1H, J=6.8 Hz), 7.29 (s, 1H), 7.31 (s, 1H), 9.81 (s, 1H).

후처리

  1. stirringThe reaction was stirred at room temperature for one hour
  2. customwas quenched by the addition of saturated aqueous NH4Cl (10 mL)
  3. customThe layers were separated
  4. extractionthe aqueous solution was extracted with EtAOc (10 mL×2)
  5. dry with materialThe combined organic solution was dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure
  8. customPurification by flash column chromatography on silica (hexane/EtOAc, 1:1)

출처 및 근거

ORD 기록
ord-65d326b3e407457bab4b28920c42aad7
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07354934B2

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