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Diethyl {[di(prop-2-en-1-yl)amino]methyl}phosphonate → Diethyl [(1H-pyrrol-1-yl)methyl]phosphonate

HRID 2247148
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HRID 2247148 반응식
[CH2:1]([N:4]([CH2:8][P:9](=[O:16])([O:13][CH2:14][CH3:15])[O:10][CH2:11][CH3:12])[CH2:5][CH:6]=[CH2:7])C=C>ClC1C=CC=CC=1>[N:4]1([CH2:8][P:9](=[O:16])([O:10][CH2:11][CH3:12])[O:13][CH2:14][CH3:15])[CH:1]=[CH:7][CH:6]=[CH:5]1
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참가 물질

3

반응물 1

HCID 15250413Diethyl {[di(prop-2-en-1-yl)amino]methyl}phosphonate

생성물 1

HCID 12901830Diethyl [(1H-pyrrol-1-yl)methyl]phosphonate수율 45%

시약·촉매·용매 1

HCID 7964Chlorobenzene용매

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온도
60 °C

실험 절차

0.1 g (0.41 mmole) of the diethyl diallylaminomethylphosphonate prepared in example 25 was dissolved in 2 ml chlorobenzene, then 0.014 g (0.02 mmole) of the bimetallic ruthenium complex 3.e prepared in example 24 was added and the mixture was stirred for 16 hours at 60° C. The catalyst was removed after evaporation of the chlorobenzene by column chromatography, yielding 0.04 g (0.18 mmole, yield 45%) diethyl 1H-pyrrole-1-ylmethylphosphonate. This product was further characterised by the following spectra:

후처리

  1. customThe catalyst was removed
  2. customafter evaporation of the chlorobenzene by column chromatography

출처 및 근거

ORD 기록
ord-2aa35d15fdfb4201b8aba3084e1d5d09
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07687635B2

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