Triethylamine → Diethyl 2-(chlorosulfonylamino)ethylphosphonate

HRID 45671

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HRID 45671 반응식
[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]

참가 물질

5

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온도
0 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-9829e9d7c4f541e9ae0a3a99bd622009
출처 데이터셋
uspto-grants-2013_09
특허 번호
US08541448B2

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