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Sodium Azide → Diethyl 3-(2-(2-azidoethoxy)ethoxy)-1,1-difluoropropylphosphonate

HRID 2204951
ノート
印刷プレビュー

反応式

HRID 2204951 の反応式
[F:1][C:2]([P:13](=[O:20])([O:17][CH2:18][CH3:19])[O:14][CH2:15][CH3:16])([F:12])[CH2:3][CH2:4][O:5][CH2:6][CH2:7][O:8][CH2:9][CH2:10]I.[N-:21]=[N+:22]=[N-:23].[Na+]>CN(C=O)C.C(OCC)(=O)C>[N:21]([CH2:10][CH2:9][O:8][CH2:7][CH2:6][O:5][CH2:4][CH2:3][C:2]([P:13](=[O:20])([O:17][CH2:18][CH3:19])[O:14][CH2:15][CH3:16])([F:12])[F:1])=[N+:22]=[N-:23]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 33557Sodium AzideHCID 58166512Diethyl 1,1-difluoro-3-(2-(2-iodoethoxy)ethoxy)propylphosphonate

生成物 1

HCID 86678262Diethyl 3-(2-(2-azidoethoxy)ethoxy)-1,1-difluoropropylphosphonate

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

To a solution of diethyl 1,1-difluoro-3-(2-(2-iodoethoxy)ethoxy)propylphosphonate (1 eq) in DMF (0.5 M) was added sodium azide (3 eq). The reaction mixture was stirred at room temperature for 90 minutes. The mixture was diluted with ethyl acetate, and washed with water. The aqueous phases were back extracted with ethyl acetate. The combined organic phases were washed with brine, dried over anhydrous Na2SO4, and concentrated en vaccuo. The crude mixture was purified by flash chromatography on a COMBIFLASH® system (ISCO) using 10-50% EtOAc/Hex to give the product as a yellowish oil.

後処理

  1. washwashed with water
  2. extractionThe aqueous phases were back extracted with ethyl acetate
  3. washThe combined organic phases were washed with brine
  4. dry with materialdried over anhydrous Na2SO4
  5. concentrationconcentrated en vaccuo
  6. customThe crude mixture was purified by flash chromatography on a COMBIFLASH® system (ISCO)

出典と根拠

ORDレコード
ord-755c5f2675e44188a6bacc66028ca4a6
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09365506B2

反応ノート

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