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

HRID 2247147
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HRID 2247147 반응식
C(NC[CH2:6][P:7](=[O:14])([O:11][CH2:12][CH3:13])[O:8][CH2:9][CH3:10])C=C.C([N:17]([CH2:20][CH3:21])CC)C.[CH2:22](Br)[CH:23]=[CH2:24].O.[CH2:27](OCC)C>>[CH2:22]([N:17]([CH2:6][P:7](=[O:14])([O:8][CH2:9][CH3:10])[O:11][CH2:12][CH3:13])[CH2:20][CH:21]=[CH2:27])[CH:23]=[CH2:24]
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참가 물질

6

반응물 5

HCID 962WaterHCID 3283Diethyl EtherHCID 7841Allyl bromideHCID 8471TriethylamineHCID 54407134HCID 54407134, 화합물

생성물 1

HCID 15250413Diethyl {[di(prop-2-en-1-yl)amino]methyl}phosphonate수율 84%

실험 절차

0.60 g (2.9 mmole) of diethyl allylaminoethylphosphonate was dissolved in 50 ml dry diethyl ether, and 1.17 g (11.6 mmole) triethylamine was added. After 15 minutes of stirring at room temperature, 1.40 g of allylbromide was added dropwise. The mixture was refluxed during 4 days. 50 ml of water was added to the mixture and was subsequently extracted three times with 50 ml CH2Cl2. The organic layers were combined and dried with MgSO4. After filtering MgSO4 and subsequent evaporation of the solvent, the resulting product was further purified with high vacuum distillation, providing 0,6 gram (2,4 mmole, 84% yield) diethyl diallylaminomethylphosphonate having a boiling point of 65° C. under a reduced pressure of 0.1 mbar. This product was further characterised by the following spectra:

후처리

  1. temperatureThe mixture was refluxed during 4 days
  2. extractionwas subsequently extracted three times with 50 ml CH2Cl2
  3. dry with materialdried with MgSO4
  4. filtrationAfter filtering
  5. customMgSO4 and subsequent evaporation of the solvent
  6. distillationthe resulting product was further purified with high vacuum distillation

출처 및 근거

ORD 기록
ord-65b695040f704b98bc2c715e950a08c2
출처 데이터셋
uspto-grants-2010_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07687635B2

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