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Methanol → Methyl 5-methoxy-1-benzofuran-2-carboxylate

HRID 1173795
ノート
印刷プレビュー

反応式

HRID 1173795 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[O:10][C:9]([C:11]([OH:13])=[O:12])=[CH:8][C:7]=2[CH:14]=1.[CH3:15]O.S(Cl)(Cl)=O>O>[CH3:15][O:12][C:11]([C:9]1[O:10][C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:14][C:7]=2[CH:8]=1)=[O:13]
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 3

HCID 887MethanolHCID 24386Thionyl ChlorideHCID 2886385-Methoxybenzofuran-2-carboxylic acid

生成物 1

HCID 14916651Methyl 5-methoxy-1-benzofuran-2-carboxylate

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

5-Methoxybenzofuran-2-carboxylic acid (5.04 g, 26 mmol) was weighed into a 200 ml round bottom flask fitted with a stir bar, septum and nitrogen inlet. Anhydrous MeOH (50 ml) was added under nitrogen atmosphere. The solution was cooled in an ice bath and thionyl chloride (2.3 ml, 32 mmol) was added dropwise with vigorous stirring. After stirring for 72 h at room temperature, the reaction mixture was poured into water (150 ml) and the white solid was collected. The solid was dissolved in toluene (100 ml) and the solution was washed with 1M NaHCO3 and brine and dried over MgSO4. Removal of the organic layer provided 5-methoxybenzofuran-2-carboxylic acid methyl ester as a white solid (5.15 g).

後処理

  1. customfitted with a stir bar
  2. temperatureThe solution was cooled in an ice bath
  3. customthe white solid was collected
  4. dissolutionThe solid was dissolved in toluene (100 ml)
  5. washthe solution was washed with 1M NaHCO3 and brine
  6. dry with materialdried over MgSO4
  7. customRemoval of the organic layer

出典と根拠

ORDレコード
ord-2921e761a43c46b2bdbee0791be185a6
出典データセット
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07834054B2

反応ノート

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