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Methyl 3-benzyloxy-5-phenylbenzoate → Methyl 3-hydroxy-5-phenylbenzoate

HRID 399851
ノート
印刷プレビュー

反応式

HRID 399851 の反応式
C([O:8][C:9]1[CH:10]=[C:11]([CH:16]=[C:17]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:18]=1)[C:12]([O:14][CH3:15])=[O:13])C1C=CC=CC=1>C(O)(=O)C.[Pd]>[OH:8][C:9]1[CH:10]=[C:11]([CH:16]=[C:17]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:18]=1)[C:12]([O:14][CH3:15])=[O:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 18945315Methyl 3-benzyloxy-5-phenylbenzoate

生成物 1

HCID 18945322Methyl 3-hydroxy-5-phenylbenzoate

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 176Acetic Acid溶媒

実験手順

To a solution of methyl 3-benzyloxy-5-phenylbenzoate (10 g) in acetic acid (300 ml) was added 10% palladium on carbon (1 g), and the mixture was subjected to catalytic hydrogenation at 80° C. under atmospheric pressure. The catalyst was removed by filtration and the filtrate was evaporated in vacuo. To the residue were added ethyl acetate and water, and adjusted to pH 5 with potassium carbonate. The separated organic layer was washed with brine, dried over magnesium sulfate and evaporated in vacuo to give methyl 3-hydroxy-5-phenylbenzoate.

後処理

  1. customwas subjected to catalytic hydrogenation at 80° C. under atmospheric pressure
  2. customThe catalyst was removed by filtration
  3. customthe filtrate was evaporated in vacuo
  4. additionTo the residue were added ethyl acetate and water
  5. washThe separated organic layer was washed with brine
  6. dry with materialdried over magnesium sulfate
  7. customevaporated in vacuo

出典と根拠

ORDレコード
ord-c3fa27934c0e4a19b3b704796311bb8e
出典データセット
uspto-grants-1998_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05824691

反応ノート

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