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Hydrochloric Acid → 12-Methoxyoctadec-9-enoic acid

HRID 1291691
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HRID 1291691 반응식
[CH3:1][O:2][CH:3]([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH2:4][CH:5]=[CH:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([O:16]CC)=[O:15].C(O)C.[OH-].[K+].Cl>CCCCCC>[CH3:1][O:2][CH:3]([CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH2:4][CH:5]=[CH:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][C:14]([OH:16])=[O:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 14797Potassium HydroxideHCID 54363898HCID 54363898, 화합물

생성물 1

HCID 5440421812-Methoxyoctadec-9-enoic acid수율 93.3%

시약·촉매·용매 1

HCID 8058Hexane용매

반응 조건

온도
50 °C

실험 절차

Next, to a 1-l flask equipped with a stirrer, 68.1 g (0.2 mol) of ethyl 12-methoxy-9-octadecenoate, 600 ml of ethanol and 45 g of a 50% aqueous solution of potassium hydroxide were charged, followed by stirring at 50° C. for 4 hours. To the reaction mixture so obtained, hexane was added, followed by neutralization with 3N hydrochloric acid and then washing with saturated saline. After concentration under reduced pressure, the residue was purified by chromatography on a silica gel column, whereby 58.3 g of the title compound (8-d) were obtained (yield: 93%).

후처리

  1. customNext, to a 1-l flask equipped with a stirrer
  2. customTo the reaction mixture so obtained
  3. washwashing with saturated saline
  4. concentrationAfter concentration under reduced pressure
  5. customthe residue was purified by chromatography on a silica gel column

출처 및 근거

ORD 기록
ord-9b254e8102c54152bdd56b97bedb6342
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05753707

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