Dimethyl malonate → 2-Diazonio-1,3-dimethoxy-3-oxoprop-1-en-1-olate

HRID 456182

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HRID 456182 반응식
[C:1]([O:8][CH3:9])(=[O:7])[CH2:2][C:3]([O:5][CH3:6])=[O:4].C(N(CC)CC)C.C1(C)C=CC(S([N:26]=[N+:27]=[N-])(=O)=O)=CC=1>CC#N>[CH3:6][O:5][C:3](=[O:4])[C:2](=[N+:26]=[N-:27])[C:1]([O:8][CH3:9])=[O:7]

참가 물질

5

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온도
39 °C

실험 절차

9.9 g. (0.075 mole) of dimethyl malonate, 50 ml of anhydrous acetonitrile, and 7.6 g (0.075 mole) of triethylamine (b.p. 88.5-90.5° C.) were added to a 300 ml double-jacketed flask with a dropping funnel, reflux condenser and mechanical stirrer (Rushton). The temperature of the mixture was adjusted to 20° C., and 14.8 g (0.075 mole) of p-toluenesulfonyl azide in 50 ml of CH3CN is added dropwise with vigorous stirring over 15 minutes. The addition caused the reaction mixture to warm to 38-40° C. and assume a yellow colour. After the mixture had been stirred at room temperature for 2.5 hours, the solvent was evaporated at 35° C. (12 mm). The partially crystalline residue was triturated with 100 ml of ether, and the mixture, including the insoluble residue, was placed in a 500 ml separatory funnel. The mixture was washed successively with a 50 ml solution of potassium hydroxide (2N) and a 50 ml solution of potassium hydroxide (0.5N) solution. The yellow-orange ethereal phase was dried over anhydrous sodium sulfate, and the solvent evaporated at 35° (15 mm) until the residue had attained a constant weight. The yellow-orange diazo ester weighed 5 g. The product was checked by 1HNMR spectroscopy and found to be ca. 90% pure.

후처리

  1. temperaturereflux condenser and mechanical stirrer (Rushton)
  2. customwas adjusted to 20° C.
  3. additionThe addition
  4. stirringAfter the mixture had been stirred at room temperature for 2.5 hours
  5. customthe solvent was evaporated at 35° C. (12 mm)
  6. customThe partially crystalline residue was triturated with 100 ml of ether
  7. customwas placed in a 500 ml separatory funnel
  8. washThe mixture was washed successively with a 50 ml solution of potassium hydroxide (2N)
  9. dry with materialThe yellow-orange ethereal phase was dried over anhydrous sodium sulfate
  10. customthe solvent evaporated at 35° (15 mm) until the residue

출처 및 근거

ORD 기록
ord-12c42106619a4267b49f40db324031d6
출처 데이터셋
uspto-grants-2013_07
특허 번호
US08497384B2

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