Heptane → Methyl 6-bromohex-2-enoate

HRID 1513541노트

반응식

HRID 1513541 반응식
[CH3:1][O:2][C:3](=[O:10])[CH:4]=[CH:5][CH2:6][CH2:7][CH2:8]Cl.[Br-:11].[Li+].CCCCCCC>O>[CH3:1][O:2][C:3](=[O:10])[CH:4]=[CH:5][CH2:6][CH2:7][CH2:8][Br:11]

참가 물질

5

실험 절차

In an atmosphere of nitrogen, 6-chloro-2-hexenoic acid methyl ester (4Cl); 188.8 g {GC purity; 83.6%, pure amount; 157.9 g (0.971 mol)}, lithium bromide (126.5 g, 1.457 mol) and heptane (16 ml) were added to a 500 ml capacity flask, followed by stirring for 6 hours under heptane reflux. After completion of the reaction, heptane was added as an extraction solvent and water was added thereto to separate the organic layer. The solvent was evaporated under a reduced pressure using an evaporator, and then the residue was distilled under a reduced pressure (70 to 80° C./0.1 ton) to obtain 6-bromo-2-hexenoic acid methyl ester (4Br); 203.4 g {GC purity; 82.3%, pure amount (4Br); 167.5 g (0.809 mol, yield 83%/(4Cl)}.

후처리

  1. temperaturereflux
  2. additionwas added
  3. customto separate the organic layer
  4. customThe solvent was evaporated under a reduced pressure
  5. customan evaporator
  6. distillationthe residue was distilled under a reduced pressure (70 to 80° C./0.1 ton)

출처 및 근거

ORD 기록
ord-fc2f0be483fc4e008a53d25faa8aa40b
출처 데이터셋
uspto-grants-2012_07
특허 번호
US08217192B2

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