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Methanol → HCID 131729111、化合物

HRID 1673422
ノート
印刷プレビュー

反応式

HRID 1673422 の反応式
CO.C(N[C:12]1[CH:20]=[C:19](/[CH:21]=[CH:22]/[C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[OH:29])[CH:18]=[CH:17][C:13]=1C(O)=O)(=O)C1C=CC=CC=1.[C:30]([O:33]CC)(=[O:32])C>[C].[Pd]>[OH:29][C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][C:23]=1[C:22]1[C:13]([CH2:12][CH3:20])=[C:17]([CH:18]=[CH:19][CH:21]=1)[C:30]([OH:33])=[O:32]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 887MethanolHCID 8857Ethyl AcetateHCID 57879342HCID 57879342、化合物

生成物 1

HCID 131729111HCID 131729111、化合物

試薬・触媒・溶媒 1

HCID 178418390HCID 178418390、化合物触媒3 回

実験手順

12 mg of 5% palladium-carbon was added to a mixed solution of 1.5 mL of methanol and 1.5 mL of ethyl acetate containing 60 mg of 2-(benzamido)-4-((E)-2-(2-hydroxyphenyl)vinyl)benzoic acid and stirred under hydrogen atmosphere at room temperature for 3 hours and minutes. 6.0 mg of 5% palladium-carbon was added to the reaction mixture and stirred under hydrogen atmosphere at room temperature for 3 hours and 20 minutes. 6.0 mg of 5% palladium-carbon was added to the reaction mixture and stirred under hydrogen atmosphere at room temperature for 2 hours and 40 minutes. Insoluble were removed by filtration and the solvent was evaporated under reduced pressure. Diisopropyl ether was added to the obtained residue and a solid substance was separated by filtration to obtain 47 mg of 2-(benzamido)-4-(2-(2-hydroxyphenyl(ethyl)benzoic acid as white solid.

後処理

  1. stirringstirred under hydrogen atmosphere at room temperature for 3 hours and 20 minutes
  2. stirringstirred under hydrogen atmosphere at room temperature for 2 hours and 40 minutes
  3. customInsoluble were removed by filtration
  4. customthe solvent was evaporated under reduced pressure
  5. additionDiisopropyl ether was added to the obtained residue
  6. customa solid substance was separated by filtration

出典と根拠

ORDレコード
ord-9a9e5e22af0a437fa80d5797f0bc0203
出典データセット
uspto-grants-2011_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07999132B2

反応ノート

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