Acetic Acid → Ethyl 2,4-dimethyl-2-pentenoate

HRID 131089

반응식

HRID 131089 반응식
[CH3:1][CH2:2][O:3][C:4]([CH:6](P(OCC)(OCC)=O)[CH3:7])=[O:5].[H-].[Na+].[CH3:18][CH:19]([CH:21]=O)[CH3:20].CC(O)=O>C(COC)OC>[CH2:2]([O:3][C:4](=[O:5])[C:6]([CH3:7])=[CH:18][CH:19]([CH3:21])[CH3:20])[CH3:1]

참가 물질

6

실험 절차

Within a period of 90 min., a solution of triethyl 2-phosphonopropionate (238 g, 1.00 mol) in dimethoxyethane (DME, 150 ml) was added dropwise with stirring under an atmosphere of N2 to a solution of NaH (43.6 g, 1.00 mol) in DME (600 ml). The mixture was then heated to reflux, and after 15 min. at reflux temp., isobutyric aldehyde (72.1 g, 1.00 mol) was added dropwise. After a further 30 min. stirring at reflux, the mixture was poured into ice/water (1:1, 1 L). AcOH (60 ml) was added, and the product was extracted with Et2O (2×200 ml). The combined organic extracts were washed with water (400 ml) and brine (100 ml), dried (Na2SO4), and concentrated in a rotary evaporator. The resulting residue was distilled to provide at 86-75° C./27 mbar 117 g (75%) of 2,4-dimethylpent-2-enoic acid ethyl ester.

후처리

  1. temperatureThe mixture was then heated
  2. temperatureto reflux
  3. temperatureafter 15 min. at reflux temp
  4. temperatureat reflux
  5. extractionthe product was extracted with Et2O (2×200 ml)
  6. washThe combined organic extracts were washed with water (400 ml) and brine (100 ml)
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated in a rotary evaporator
  9. distillationThe resulting residue was distilled

출처 및 근거

ORD 기록
ord-461ef08b6d284852ae374eeeb9552cd8
출처 데이터셋
uspto-grants-2008_06
특허 번호
US07384906B2

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