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Methyl 4-benzyloxy-5-isopropyl-2-methoxybenzoate → Methyl 4-hydroxy-5-isopropyl-2-methoxybenzoate

HRID 1182792
ノート
印刷プレビュー

反応式

HRID 1182792 の反応式
C([O:8][C:9]1[C:18]([CH:19]([CH3:21])[CH3:20])=[CH:17][C:12]([C:13]([O:15][CH3:16])=[O:14])=[C:11]([O:22][CH3:23])[CH:10]=1)C1C=CC=CC=1>[Pd].CO>[OH:8][C:9]1[C:18]([CH:19]([CH3:21])[CH3:20])=[CH:17][C:12]([C:13]([O:15][CH3:16])=[O:14])=[C:11]([O:22][CH3:23])[CH:10]=1
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 58236472Methyl 4-benzyloxy-5-isopropyl-2-methoxybenzoate

生成物 1

HCID 58236464Methyl 4-hydroxy-5-isopropyl-2-methoxybenzoate収率 97%

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

10% Palladium on carbon (80 mg) was added to a suspension of methyl 4-benzyloxy-5-isopropyl-2-methoxybenzoate (624 mg, 1.99 mmol) in methanol (16 ml) and the mixture was stirred at room temperature under a hydrogen atmosphere for 3 hours. The mixture was filtered, the catalyst was rinsed with methanol (3×5 ml) and the combined filtrates were evaporated in vacuo to afford methyl 4-hydroxy-5-isopropyl-2-methoxybenzoate (432 mg, 97%) as an off-white solid. 1H NMR (DMSO-d6) 10.18 (1H, br s), 7.52 (1H, s), 6.52 (1H, s), 3.73 (3H, s), 3.71 (3H, s), 3.11 (1H, m), 1.14 (6H, d). MS: [M+Na]+ 247.

後処理

  1. filtrationThe mixture was filtered
  2. washthe catalyst was rinsed with methanol (3×5 ml)
  3. customthe combined filtrates were evaporated in vacuo

出典と根拠

ORDレコード
ord-bcbdff09fd304b61b91f9d7965c0291f
出典データセット
uspto-grants-2014_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08664218B2

反応ノート

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