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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → 2-(3,4,5-Trimethoxyphenyl)benzyl Alcohol

HRID 1634867
ノート
印刷プレビュー

反応式

HRID 1634867 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13]2[CH:23]=[CH:22][CH:21]=[CH:20][C:14]=2[C:15](OCC)=[O:16])[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].[H-].[Al+3].[Li+].[H-].[H-].[H-].O.S([O-])([O-])(=O)=O.[Na+].[Na+]>C1COCC1>[CH3:12][O:11][C:7]1[CH:6]=[C:5]([C:13]2[CH:23]=[CH:22][CH:21]=[CH:20][C:14]=2[CH2:15][OH:16])[CH:4]=[C:3]([O:2][CH3:1])[C:8]=1[O:9][CH3:10]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 24436Sodium SulfateHCID 21226445Aluminium lithium hydrideHCID 22558004Ethyl 2-(3,4,5-trimethoxyphenyl)benzoate

生成物 1

HCID 213388232-(3,4,5-Trimethoxyphenyl)benzyl Alcohol

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
0 °C

実験手順

Ethyl 2-(3,4,5-trimethoxyphenyl)benzoate (655 mg) was dissolved in THF (20 mL), and to the solution lithium aluminum hydride (80 mg) was added at 0° C. under an argon atmosphere. The mixture was stirred at 0° C. for 1 hour as it is. A small amount of water and then sodium sulfate were added to the reaction mixture, and the reaction mixture was filtered through celite. The filtrate was concentrated under reduced pressure, and the resultant crude crystals were recrystallized from ethyl acetate-hexane to obtain the title compound.

後処理

  1. filtrationthe reaction mixture was filtered through celite
  2. concentrationThe filtrate was concentrated under reduced pressure
  3. customthe resultant crude crystals were recrystallized from ethyl acetate-hexane

出典と根拠

ORDレコード
ord-ab6688c5a4c041a18cf40270231b93ac
出典データセット
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06509329B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート