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1-benzyl-1H-pyrrole-2-carbaldehyde → 1-(1-benzyl-1H-pyrrol-2-yl)-2-methylpropan-1-ol

HRID 748072
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반응식

HRID 748072 반응식
[CH2:1]([N:8]1[CH:12]=[CH:11][CH:10]=[C:9]1[CH:13]=[O:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH:15]([Mg]Br)([CH3:17])[CH3:16]>C1COCC1>[CH2:1]([N:8]1[CH:12]=[CH:11][CH:10]=[C:9]1[CH:13]([OH:14])[CH:15]([CH3:17])[CH3:16])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1
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참가 물질

4

반응물 2

HCID 111269641-benzyl-1H-pyrrole-2-carbaldehydeHCID 178418365HCID 178418365, 화합물

생성물 1

HCID 685935001-(1-benzyl-1H-pyrrol-2-yl)-2-methylpropan-1-ol수율 56%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To 1-benzyl-1H-pyrrole-2-carbaldehyde (0.50 g, 2.7 mmol) in THF (20 mL) at 0° C. was added a solution of i-PrMgBr (5.4 mL, 1N in THF, 5.4 mmol). The reaction mixture was warmed to room temperature and after 1.5 h it was quenched with saturated aqueous ammonium chloride, extracted with EtOAc, dried (Na2SO4) and concentrated. Column chromatography (EtOAc/hexanes, 1:4) provided 0.345 g (56%) of 1-(1-benzyl-1H-pyrrol-2-yl)-2-methylpropan-1-ol as an oil.

후처리

  1. customwas quenched with saturated aqueous ammonium chloride
  2. extractionextracted with EtOAc
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8783486082344aa09ca65b33ff87acb1
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07399778B2

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