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Ethyl 2-methyl-3,4-pentadienoate → ethyl (2E)-2-methylpenta-2,4-dienoate

HRID 1749117
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HRID 1749117 반응식
[O-]CC.[Na+].[CH3:5][CH:6]([CH:12]=[C:13]=[CH2:14])[C:7]([O:9][CH2:10][CH3:11])=[O:8]>C(O)C>[CH3:5]/[C:6](=[CH:12]\[CH:13]=[CH2:14])/[C:7]([O:9][CH2:10][CH3:11])=[O:8]
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참가 물질

4

반응물 2

HCID 62166Ethyl 2-methyl-3,4-pentadienoateHCID 2723922Sodium ethoxide

생성물 1

HCID 6372304ethyl (2E)-2-methylpenta-2,4-dienoate

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Sodium ethoxide solution (21% in ethanol, 33.3 ml, cat.) was added to a solution of ethyl 2-methylpenta-3,4-dienoate (Bedoukian, 125.0 g, 890 mmol) in anhydrous ethanol (350 ml) and stirred at ambient temperature for 12 hours. The solution was concentrated in vacuo and the residue partitioned between ether and saturated NH4Cl solution. The aqueous phase was re-extracted twice with ether, then the combined organic phase washed with NH4Cl and then brine, dried over Na2SO4, filtered and the solvents removed in vacuo to yield the crude ester, 125.8 g as an orange oil which was used directly in the next step without further purification.

후처리

  1. concentrationThe solution was concentrated in vacuo
  2. customthe residue partitioned between ether and saturated NH4Cl solution
  3. extractionThe aqueous phase was re-extracted twice with ether
  4. washthe combined organic phase washed with NH4Cl
  5. dry with materialbrine, dried over Na2SO4
  6. filtrationfiltered
  7. customthe solvents removed in vacuo

출처 및 근거

ORD 기록
ord-327c38d476ca44b78c732aec9b390698
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09156770B2

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