Triethylamine → Diethyl 2-(chlorosulfonylamino)ethylphosphonate

HRID 45671ノート

反応式

HRID 45671 の反応式
[S:1]([Cl:5])(Cl)(=[O:3])=[O:2].[NH2:6][CH2:7][CH2:8][P:9](=[O:16])([O:13][CH2:14][CH3:15])[O:10][CH2:11][CH3:12].C(N(CC)CC)C>ClCCl>[Cl:5][S:1]([NH:6][CH2:7][CH2:8][P:9](=[O:16])([O:10][CH2:11][CH3:12])[O:13][CH2:14][CH3:15])(=[O:3])=[O:2]

参加物

5

反応条件

温度
0 °C

実験手順

Into a 100-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of sulfuryl dichloride (1.1 g, 8.15 mmol, 1.47 equiv) in dichloromethane (10 mL). This was followed by the addition of a solution of diethyl 2-aminoethylphosphonate (intermediate 1.9) (1.0 g, 5.52 mmol, 1.00 equiv) and triethylamine (800 mg, 7.92 mmol, 1.43 equiv) in dichloromethane (20 mL) dropwise with stirring at 0° C. The resulting solution was stirred for 2 h at 0° C. The reaction was then quenched by the addition of ice water. The organic layer was washed with saturated sodium chloride (20 mL), dried over anhydrous sodium sulfate and concentrated under vacuum. This resulted in 0.5 g (crude) of the title compound as a colorless oil.

後処理

  1. customInto a 100-mL round-bottom flask purged
  2. temperaturemaintained with an inert atmosphere of nitrogen
  3. stirringThe resulting solution was stirred for 2 h at 0° C
  4. customThe reaction was then quenched by the addition of ice water
  5. washThe organic layer was washed with saturated sodium chloride (20 mL)
  6. dry with materialdried over anhydrous sodium sulfate
  7. concentrationconcentrated under vacuum

出典と根拠

ORDレコード
ord-9829e9d7c4f541e9ae0a3a99bd622009
出典データセット
uspto-grants-2013_09
特許番号
US08541448B2

反応ノート

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