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Methylamine → 3-(benzyloxy)-N-methylpropan-1-amine

HRID 1837269
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HRID 1837269 반응식
[CH3:1][NH2:2].Br[CH2:4][CH2:5][CH2:6][O:7][CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>O1CCCC1>[CH2:8]([O:7][CH2:6][CH2:5][CH2:4][NH:2][CH3:1])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1
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참가 물질

4

반응물 2

HCID 6329Methylamine2회HCID 2776064Benzyl 3-Bromopropyl Ether

생성물 1

HCID 234970393-(benzyloxy)-N-methylpropan-1-amine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

3.57 g of methylamine is condensed in a solution of 1.8 ml of (3-bromo-propoxymethyl)-benzene in 15 ml of anhydrous tetrahydrofuran at −78° C., and it is stirred overnight at room temperature in a pressurized reactor. After the pressurized reactor was opened at −20° C., it is allowed to come to room temperature to allow excess methylamine to evaporate off. Then, the reaction solution is added to saturated sodium chloride solution, extracted with ether, dried on magnesium sulfate and concentrated by evaporation in a vacuum. 1.91 g of (3-benzyloxy-propyl)-methyl-amine is obtained as a crude product, which is used without further purification in the next stage.

후처리

  1. customwas opened at −20° C.
  2. customto come to room temperature
  3. customto evaporate off
  4. additionThen, the reaction solution is added to saturated sodium chloride solution
  5. extractionextracted with ether
  6. customdried on magnesium sulfate
  7. concentrationconcentrated by evaporation in a vacuum

출처 및 근거

ORD 기록
ord-0fbd7af9fbb546fe9f252085efa052d8
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06780855B2

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