Sodium Methoxide → Methyl 6-hydroxy-1,4-benzodioxin-2-carboxylate

HRID 1756032ノート

反応式

HRID 1756032 の反応式
C[O-].[Na+].C([O:7][C:8]1[CH:22]=[CH:21][C:11]2[O:12][C:13]([C:16]([O:18][CH2:19]C)=[O:17])=[CH:14][O:15][C:10]=2[CH:9]=1)(=O)C>CO>[OH:7][C:8]1[CH:22]=[CH:21][C:11]2[O:12][C:13]([C:16]([O:18][CH3:19])=[O:17])=[CH:14][O:15][C:10]=2[CH:9]=1

参加物

4

反応物 2

HCID 10942334Sodium MethoxideHCID 11043631HCID 11043631、化合物

生成物 1

HCID 19392464Methyl 6-hydroxy-1,4-benzodioxin-2-carboxylate収率 87%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Add 3.8 mmol of a 2M solution of sodium methanolate to a solution of 0.38 mmol of ethyl 6-acetoxy-1,4-benzodioxin-2-carboxylate in 5 cm3 of anhydrous methanol. After stirring for 4 hours at room temperature and neutralising with acid Dowex resin, the reaction mixture is concentrated under reduced pressure and the crude product obtained is purified by chromatography on a silica column (eluant: petroleum ether/diethyl ether, 80:20). Methyl 6-hydroxy-1,4-benzodioxin-2-carboxylate is thereby obtained in a yield of 87%.

後処理

  1. concentrationthe reaction mixture is concentrated under reduced pressure
  2. customthe crude product obtained
  3. customis purified by chromatography on a silica column (eluant: petroleum ether/diethyl ether, 80:20)

出典と根拠

ORDレコード
ord-295ece9631ee44eaad2a34b2fe24bbd3
出典データセット
uspto-grants-1995_08
特許番号
US05439909

反応ノート

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