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HCID 58236461、化合物 → Methyl 4-hydroxy-5-isopropyl-2-(methoxymethyloxy)benzoate

HRID 389965
ノート
印刷プレビュー

反応式

HRID 389965 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][CH2:23][O:24][CH3:25])[CH:10]=1)C1C=CC=CC=1>CO.[Pd]>[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][CH2:23][O:24][CH3:25])[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 58236461HCID 58236461、化合物

生成物 1

HCID 58236469Methyl 4-hydroxy-5-isopropyl-2-(methoxymethyloxy)benzoate

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

The crude methyl 4-benzyloxy-5-isopropyl-2-(methoxymethyloxy)benzoate was dissolved in methanol (20 ml), 10% palladium on carbon (160 mg) was added and the mixture was stirred at room temperature under a hydrogen atmosphere for 16 hours. The mixture was filtered, the catalyst was rinsed with methanol (3×5 ml) and the combined filtrates were evaporated in vacuo to afford crude methyl 4-hydroxy-5-isopropyl-2-(methoxymethyloxy)benzoate as a colourless oily solid that was used in the next step without further purification. 1H NMR (DMSO-d6) 10.19 (1H, br s), 7.52 (1H, s), 6.57 (1H, s), 5.13 (2H, s), 3.73 (3H, s), 3.40 (3H, s), 3.11 (1H, m), 1.13 (6H, d). MS: [M−H]− 253.

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-02012b883239488b987221b0ae1ec968
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08383619B2

反応ノート

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