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Hydrochloric Acid → 3-Methyl-6-hydroxybenzofuran

HRID 1107864
ノート
印刷プレビュー

反応式

HRID 1107864 の反応式
[OH:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][CH:12]=1)[O:5][CH2:6][C:7](=O)[CH3:8].[OH-].[K+].Cl>>[CH3:8][C:7]1[C:10]2[CH:11]=[CH:12][C:2]([OH:1])=[CH:3][C:4]=2[O:5][CH:6]=1
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

4

反応物 3

HCID 313Hydrochloric AcidHCID 14797Potassium HydroxideHCID 18786125(3-Hydroxyphenoxy)acetone

生成物 1

HCID 108556243-Methyl-6-hydroxybenzofuran収率 60.4%

反応条件

温度
5 °C

実験手順

3 g (18 mmol) of (3-hydroxyphenoxy)acetone and 400 ml of a 0.1M potassium hydroxide solution are introduced into a 1 l three-necked flask equipped with a reflux condenser. Heating is carried out at reflux for 6 hours. The reaction mixture is cooled to 5° C., a molar hydrochloric acid solution is added, in order to obtain a pH of approximately 5, and extraction is carried out with ethyl ether (3×150 ml). The organic phases are combined, dried over magnesium sulphate and concentrated. The residue is purified by silica column chromatography (elution solvent: 8/2 cyclohexane/ethyl acetate). 1.61 g of 3-methyl-6-hydroxybenzofuran are obtained--M.p.: 92° C.

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

後処理

  1. customequipped with a reflux condenser
  2. temperatureHeating
  3. temperatureat reflux for 6 hours
  4. customto obtain
  5. extractiona pH of approximately 5, and extraction
  6. dry with materialdried over magnesium sulphate
  7. concentrationconcentrated
  8. customThe residue is purified by silica column chromatography (elution solvent: 8/2 cyclohexane/ethyl acetate)

出典と根拠

ORDレコード
ord-80cae4e0f7424c6ea2f4512a170fc7a7
出典データセット
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06063810

反応ノート

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