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HCID 10893325、化合物 → 10-Hydroxy-9-methoxyoctadecanoic acid

HRID 2279686
ノート
印刷プレビュー

反応式

HRID 2279686 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 10893325HCID 10893325、化合物

生成物 1

HCID 1384764910-Hydroxy-9-methoxyoctadecanoic acid

試薬・触媒・溶媒 1

HCID 23721981Sodium hydroxide methanol溶媒

実験手順

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.

後処理

  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
  • 出典と根拠

    ORDレコード
    ord-001faf2151134d449a741a7f2a4e2688
    出典データセット
    uspto-grants-2015_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US09133305B2

    反応ノート

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