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Ethanolamine → 4-[3-(2-Hydroxyethylamino)propyl]benzonitrile

HRID 899133
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HRID 899133 반응식
Br[CH2:2][CH2:3][CH2:4][C:5]1[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[CH:7][CH:6]=1.[CH2:13]([CH2:15][NH2:16])[OH:14].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[OH:14][CH2:13][CH2:15][NH:16][CH2:2][CH2:3][CH2:4][C:5]1[CH:12]=[CH:11][C:8]([C:9]#[N:10])=[CH:7][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 700EthanolamineHCID 11430Potassium CarbonateHCID 4583644-(3-Bromopropyl)benzonitrile

생성물 1

HCID 690715794-[3-(2-Hydroxyethylamino)propyl]benzonitrile수율 82.5%

시약·촉매·용매 1

HCID 6342Acetonitrile용매2회

실험 절차

4-(3-Bromopropyl)benzonitrile (20 g, 0.089 mol) in acetonitrile was added to a vigorously stirred mixture of ethanolamine (27.2 g, 0.447 mol) and potassium carbonate (18.5 g, 0.133 mol) in 300 mL of dry acetonitrile. Stirring was then continued at room temperature overnight under a nitrogen atmosphere. The reaction mixture was filtered and concentrated under reduced pressure. The crude product thereby obtained was purified by column chromatography (using methanol in chloroform) to yield 15 g of the sub-title compound.

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후처리

  1. filtrationThe reaction mixture was filtered
  2. concentrationconcentrated under reduced pressure
  3. customThe crude product thereby obtained
  4. customwas purified by column chromatography (using methanol in chloroform)

출처 및 근거

ORD 기록
ord-0f28dc3322c4467c844dcfd008192dd3
출처 데이터셋
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07354917B2

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