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Hydrogen chloride-ethyl acetate → 4-(2-Hydroxyethoxy)-6-methylpyridin-3-ol

HRID 1038591
ノート
印刷プレビュー

反応式

HRID 1038591 の反応式
COC[O:4][C:5]1[C:6]([O:12][CH2:13][CH2:14][OH:15])=[CH:7][C:8]([CH3:11])=[N:9][CH:10]=1.Cl.C(OCC)(=O)C>C(OCC)(=O)C>[OH:15][CH2:14][CH2:13][O:12][C:6]1[CH:7]=[C:8]([CH3:11])[N:9]=[CH:10][C:5]=1[OH:4]
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 2

HCID 21866389Hydrogen chloride-ethyl acetateHCID 665986772-(5-(Methoxymethoxy)-2-methylpyridin-4-yloxy)ethanol

生成物 1

HCID 665990334-(2-Hydroxyethoxy)-6-methylpyridin-3-ol収率 168.1%

試薬・触媒・溶媒 1

HCID 8857Ethyl Acetate溶媒

実験手順

2-(5-(Methoxymethoxy)-2-methylpyridin-4-yloxy)ethanol (900 mg, 4.22 mmol) was dissolved in ethyl acetate (10 mL), added 4N hydrochloric acid-ethyl acetate solution (10 mL), and the mixture was stirred at room temperature for 5 hours. After the reaction has terminated, under ice-cold conditions, a 4N aqueous solution of sodium hydroxide was used to adjust the reaction solution to pH=8. The reaction solution was concentrated in vacuo. The obtained residue was washed with chloroform/methanol, dried, and as a crude product, 4-(2-hydroxyethoxy)-6-methylpyridin-3-ol (1.2 g) was obtained as a white solid.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. customAfter the reaction has terminated, under ice-cold conditions
  2. concentrationThe reaction solution was concentrated in vacuo
  3. washThe obtained residue was washed with chloroform/methanol
  4. customdried

出典と根拠

ORDレコード
ord-7c7aa91cd96b43d8bb3ca03f61598f8f
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08551985B2

反応ノート

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