Acetic Acid → Dimethyl 2-oxo-2-phenylethylphosphonate

HRID 1389029노트

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HRID 1389029 반응식
[CH3:1][P:2](=[O:7])([O:5][CH3:6])[O:3][CH3:4].P(=O)([O-])[O-].[CH2:12]([Li])[CH2:13][CH2:14]C.C(O)(=O)C.[O:21]1[CH2:25][CH2:24][CH2:23][CH2:22]1>CCCCCC>[O:21]=[C:25]([C:24]1[CH:14]=[CH:13][CH:12]=[CH:22][CH:23]=1)[CH2:1][P:2](=[O:7])([O:5][CH3:6])[O:3][CH3:4]

참가 물질

7

실험 절차

A solution of 74.5 g (600 mmoles) dimethyl methylphosphonate (Aldrich) in 750 ml dry tetrahydrofuran was cooled to -78° in a dry nitrogen atmosphere. To the stirred phosphonate solution was added 265 ml of 2.34 M n-butyllithium in hexane solution (Alfa Inorganics, Inc.) dropwise over a period of 30 minutes at such a rate that the reaction temperature never rose above -65°. After an additional 5 minutes stirring at -78°, 41 g (300 mmole) of methyl azoate was added dropwise at a rate that kept the reaction temperature less than -70° (10 minutes). After 1 hour at -78° the reaction mixture was allowed to warm to ambient temperature, neutralized with 35 ml acetic acid and rotary evaporated to a white gel. The gelatinous material was taken up in 75 ml water, the aqueous phase extracted with 300 ml portions of ether (3x), the combined organic extracts were backwashed (50 cc H2O), dried (MgSO4), and concentrated (water aspirator) to a crude residue and distilled, b.p. 130°-5° (0.04 mm) to give 35 g (29%) dimethyl 2-oxo-2-phenylethylphosphonate (2a).

후처리

  1. addition41 g (300 mmole) of methyl azoate was added dropwise at a rate that
  2. customthe reaction temperature less than -70° (10 minutes)
  3. waitAfter 1 hour at -78° the reaction mixture was allowed
  4. customrotary evaporated to a white gel
  5. extractionthe aqueous phase extracted with 300 ml portions of ether (3x)
  6. dry with materialdried (MgSO4)
  7. concentrationconcentrated (water aspirator) to a crude residue
  8. distillationdistilled

출처 및 근거

ORD 기록
ord-4b59926ac9f946be84dceb54d7de561d
출처 데이터셋
uspto-grants-1981_01
특허 번호
US04243595

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