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Triethanolamine → Ethyl 6-hydroxy-4-methylhexa-2,4-dienoate

HRID 1719107
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반응식

HRID 1719107 반응식
C([O:4][CH2:5][CH:6]=[C:7]([CH3:15])[CH:8]=[CH:9][C:10]([O:12][CH2:13][CH3:14])=[O:11])(=O)C.C(=O)([O-])[O-].[Na+].[Na+].N(CCO)(CCO)CCO.C(OCC)(=O)C>C(O)C>[OH:4][CH2:5][CH:6]=[C:7]([CH3:15])[CH:8]=[CH:9][C:10]([O:12][CH2:13][CH3:14])=[O:11]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7618TriethanolamineHCID 8857Ethyl AcetateHCID 10340Sodium CarbonateHCID 54268690Ethyl 6-(acetyloxy)-4-methylhexa-2,4-dienoate

생성물 1

HCID 54238884Ethyl 6-hydroxy-4-methylhexa-2,4-dienoate수율 71.2%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

27.5 g of ethyl 6-acetoxy-4-methyl-2,4-hexadienoate, 20 g of sodium carbonate and 2 ml of triethanolamine were heated to reflux for 3 hours in 250 ml of ethanol. After the addition of ethyl acetate, the organic phase was washed with saturated sodium chloride solution, dried over magnesium sulphate and concentrated. Distillation at 110° C./0.4 mmHg gave 15.7 g (71%) of ethyl 6-hydroxy-4-methyl-2,4-hexadienoate.

후처리

  1. washthe organic phase was washed with saturated sodium chloride solution
  2. dry with materialdried over magnesium sulphate
  3. concentrationconcentrated
  4. distillationDistillation at 110° C./0.4 mmHg

출처 및 근거

ORD 기록
ord-ea7b9da8a510461684ede7de40d5d547
출처 데이터셋
uspto-grants-1985_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04539154

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