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Methylamine → Methyl-(7,7,8,8,8-pentafluor-octyl)-amine

HRID 1837259
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반응식

HRID 1837259 반응식
[CH3:1][NH2:2].[F:3][C:4]([F:26])([C:22]([F:25])([F:24])[F:23])[CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10]C1C=C(C)C=CC=1S([O-])(=O)=O>O1CCCC1>[CH3:1][NH:2][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][C:4]([F:26])([F:3])[C:22]([F:25])([F:24])[F:23]
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참가 물질

4

반응물 2

HCID 6329Methylamine2회HCID 234970987,7,8,8,8-Pentafluor-octyltosylate

생성물 1

HCID 17910986Methyl-(7,7,8,8,8-pentafluor-octyl)-amine수율 87.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

4.0 g of methylamine is condensed in a solution of 2.9 g of 7,7,8,8,8-pentafluor-octyltosylate in 10 ml of absolute tetrahydrofuran at −20° C., and it is stirred overnight in a pressure vessel at room temperature. After the pressure vessel was opened at −20° C., it is allowed to come to room temperature to allow excess methylamine to evaporate off. The reaction solution is taken up in dichloromethane, washed with water, dried on magnesium sulfate and concentrated by evaporation in a vacuum. 1.58 g of methyl-(7,7,8,8,8-pentafluor-octyl)-amine is obtained as a crude product.

후처리

  1. customwas opened at −20° C.
  2. customto come to room temperature
  3. customto evaporate off
  4. washwashed with water
  5. customdried on magnesium sulfate
  6. concentrationconcentrated by evaporation in a vacuum

출처 및 근거

ORD 기록
ord-3d955e2e631145a1851dea85c23cc820
출처 데이터셋
uspto-grants-2004_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06780855B2

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