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HCID 10893325, 화합물 → 10-Hydroxy-9-methoxyoctadecanoic acid

HRID 2279686
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HRID 2279686 반응식
[OH:1][CH:2]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH:3]([O:15][CH3:16])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([O:13]C)=[O:12]>[OH-].[Na+].CO>[OH:1][CH:2]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH3:24])[CH:3]([O:15][CH3:16])[CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][C:11]([OH:13])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 10893325HCID 10893325, 화합물

생성물 1

HCID 1384764910-Hydroxy-9-methoxyoctadecanoic acid

시약·촉매·용매 1

HCID 23721981Sodium hydroxide methanol용매

실험 절차

The methyl 10-hydroxy-9-methoxyoctadecanoate (3) (4.0 g; 0.012 mol) was dissolved in 1N methanol sodium hydroxide solution (100 mL) (Aldrich) and heated under reflux for 12 h. The methanol was removed from the reaction mixture and the crude product was dissolved in 100 mL water. The aqueous solution was neutralised with hydrochloric acid (Aldrich) and the product extracted with 3×50 mL dichloromethane (J. T. Baker). The dichloromethane solution was washed with 3×50 mL water and dried over anhydrous sodium sulfate (J. T. Baker). The dichloromethane solution was filtered and the solvent was removed to obtain the intermediate compound 4.

후처리

  1. temperatureheated
  • temperatureunder reflux for 12 h
  • customThe methanol was removed from the reaction mixture
  • dissolutionthe crude product was dissolved in 100 mL water
  • extractionthe product extracted with 3×50 mL dichloromethane (J. T. Baker)
  • washThe dichloromethane solution was washed with 3×50 mL water
  • dry with materialdried over anhydrous sodium sulfate (J. T. Baker)
  • filtrationThe dichloromethane solution was filtered
  • customthe solvent was removed
  • 출처 및 근거

    ORD 기록
    ord-001faf2151134d449a741a7f2a4e2688
    출처 데이터셋
    uspto-grants-2015_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09133305B2

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