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Ethanol → 3-(4-Methoxyphenyl)pentanedioic acid

HRID 67200
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반응식

HRID 67200 반응식
[CH3:1][O:2][C:3]1[CH:25]=[CH:24][C:6]([CH:7]([CH:15](C(C)=O)[C:16]([O:18]CC)=[O:17])[CH:8](C(C)=O)[C:9]([O-:11])=[O:10])=[CH:5][CH:4]=1.C(O)C.[OH-].[Na+]>O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH:7]([CH2:15][C:16]([OH:18])=[O:17])[CH2:8][C:9]([OH:11])=[O:10])=[CH:24][CH:25]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 702EthanolHCID 14798Sodium HydroxideHCID 86737067Ethyl 2,2'-(4-methoxybenzal)-bis-acetoacetate2회

생성물 1

HCID 3472533-(4-Methoxyphenyl)pentanedioic acid수율 16.1%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

A mixture of ethyl 2,2'-(4-methoxybenzal)-bis-acetoacetate (30 g), ethanol (450 ml) and 50% sodium hydroxide (450 g) is refluxed vigorously for 1.0 hour. Water (150 ml) is added and most of the ethanol is removed by distillation in vacuo. The concentrate is acidified with concentrated hydrochloric acid and is extracted with ethyl acetate. The ethyl acetate solution is washed with brine, dried, evaporated and the residue is crystallized from benzene-methanol to afford 3.3 g of 3-(4-methoxyphenyl)glutaric acid, melting point 147°-150° C.

후처리

  1. temperatureis refluxed vigorously for 1.0 hour
  2. customis removed by distillation in vacuo
  3. extractionis extracted with ethyl acetate
  4. washThe ethyl acetate solution is washed with brine
  5. customdried
  6. customevaporated
  7. customthe residue is crystallized from benzene-methanol

출처 및 근거

ORD 기록
ord-ed3cc440e4dd4bb09199c0c9c613823e
출처 데이터셋
uspto-grants-1982_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04345096

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