Formaldehyde → 4-Methyl-2-methylene valeric acid

HRID 129721

반응식

HRID 129721 반응식
[CH2:1]([CH:5]([C:9](O)=O)[C:6]([OH:8])=[O:7])[CH:2]([CH3:4])[CH3:3].C=O.C(NCC)C>C(Cl)(Cl)Cl>[CH3:3][CH:2]([CH3:4])[CH2:1][C:5](=[CH2:9])[C:6]([OH:8])=[O:7]

참가 물질

5

실험 절차

To a stirred mixture of 14.0 g of isobutylmalonic acid and 37 mL of 37% formalin was added 9.05 mL of diethylamine at room temperature. The mixture was stirred at room temperature for 3 h and refluxed for an additional 2 h. The reaction mixture was cooled to room temperature and diluted with CHCl3, and extracted with saturated aqueous NaHCO3. The aqueous layer was acidified with 1M HCl and extracted with CHCl3. The organic extract was dried over anhydrous Na2SO4 and evaporated under reduced pressure to afford 11.0 g at 98% yield of 4-methyl-2-methylenepentanoic acid as a clear liquid which was used without further purification. Characteristic analytical data are as follows: 1H NMR (300 MHz, CDCl3) δ6.32 (d, J=2 Hz, 1H), 5.62 (d, J=2 Hz, 1H), 2.17 (dd, J=1, 7 Hz, 2H), 1.82 (m, 1H), 0.90 (d, J=7 Hz, 6H); 13C NMR (300 MHz) δ173.6, 139.4, 128.4, 40.7, 26.9, 22.0.

후처리

  1. temperaturerefluxed for an additional 2 h
  2. temperatureThe reaction mixture was cooled to room temperature
  3. extractionextracted with saturated aqueous NaHCO3
  4. extractionextracted with CHCl3
  5. extractionThe organic extract
  6. dry with materialwas dried over anhydrous Na2SO4
  7. customevaporated under reduced pressure

출처 및 근거

ORD 기록
ord-b2f24af807dc4038aef169fa170a7fad
출처 데이터셋
uspto-grants-1995_11
특허 번호
US05470834

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