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Sodium Hydroxide → 5,6-dimethoxy-1H-indene-2-carboxylic Acid

HRID 2175694
ノート
印刷プレビュー

反応式

HRID 2175694 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][C:11]=1[O:12][CH3:13])[CH2:8][C:7]([C:14]([O:16]C)=[O:15])=[CH:6]2.[OH-].[Na+]>C1COCC1.CO>[CH3:13][O:12][C:11]1[CH:10]=[C:9]2[C:5](=[CH:4][C:3]=1[O:2][CH3:1])[CH2:6][C:7]([C:14]([OH:16])=[O:15])=[CH:8]2
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 2

HCID 14798Sodium HydroxideHCID 12423472methyl 5,6-dimethoxy-1H-indene-2-carboxylate

生成物 1

HCID 103761625,6-dimethoxy-1H-indene-2-carboxylic Acid収率 48.3%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 8028Tetrahydrofuran溶媒

実験手順

To a stirred solution of methyl 5,6-dimethoxy-1H-indene-2-carboxylate (330 mg, 1.41 mmol) in THF (8 mL) and MeOH (4 mL) was added 2 N NaOH solution (3.5 mL) dropwise at room temperature. The resulting mixture was stirred at room temperature for 2 hours and the reaction was quenched with 1N HCl solution. Then mixture was diluted with water and the resulting suspension was filtered and the solid was dried under vacuum to give 5,6-dimethoxy-1H-indene-2-carboxylic acid (150 mg, 48%). LC-MS (ES-API); rt 8.44 min; m/z calculated for C12H12O4 [M−H]− 219.1, found 219.1.

後処理

  1. customthe reaction was quenched with 1N HCl solution
  2. additionThen mixture was diluted with water
  3. filtrationthe resulting suspension was filtered
  4. customthe solid was dried under vacuum

出典と根拠

ORDレコード
ord-b0ad512fc3d644aa91851d20b059e618
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09062076B2

反応ノート

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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