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Ethanol → Ethyl 7-acetyl-2,3-dihydro-1,4-benzodioxine-2-carboxylate

HRID 1756027
ノート
印刷プレビュー

反応式

HRID 1756027 の反応式
[C:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:12][CH2:11][CH:10]([C:13](N)=[O:14])[O:9][C:8]=2[CH:16]=1)(=[O:3])[CH3:2].[CH2:17]([OH:19])[CH3:18]>Cl>[C:1]([C:4]1[CH:5]=[CH:6][C:7]2[O:12][CH2:11][CH:10]([C:13]([O:19][CH2:17][CH3:18])=[O:14])[O:9][C:8]=2[CH:16]=1)(=[O:3])[CH3:2]
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 702EthanolHCID 181774107-Acetyl-2,3-dihydro-1,4-benzodioxin-2-carboxamide

生成物 1

HCID 13723676Ethyl 7-acetyl-2,3-dihydro-1,4-benzodioxine-2-carboxylate収率 75%

試薬・触媒・溶媒 1

HCID 313Hydrochloric Acid溶媒

実験手順

Heat a solution of 3 g (13.5 mmol) of 7-acetyl-2,3-dihydro-1,4-benzodioxin-2-carboxamide dissolved in 100 cm3 of ethanol saturated with hydrochloric acid at reflux for 18 hours under a nitrogen atmosphere. After cooling, the reaction mixture is filtered, concentrated and, after neutralisation with sodium hydrogen carbonate, extracted with methylene chloride. The crude product obtained by concentrating the organic phase to dryness is purified by chromatography on a silica column (eluant: petroleum ether/diethyl ether, 50:50). Ethyl 7-acetyl-2,3-dihydro-1,4-benzodioxin-2-carboxylate is thereby obtained in a yield of 75%. Melting point: 57° C. ##STR35##

後処理

  1. temperatureat reflux for 18 hours under a nitrogen atmosphere
  2. temperatureAfter cooling
  3. filtrationthe reaction mixture is filtered
  4. concentrationconcentrated
  5. extractionafter neutralisation with sodium hydrogen carbonate, extracted with methylene chloride
  6. customThe crude product obtained
  7. concentrationby concentrating the organic phase to dryness
  8. customis purified by chromatography on a silica column (eluant: petroleum ether/diethyl ether, 50:50)

出典と根拠

ORDレコード
ord-848e28a70b944e00ad18b80de5892a22
出典データセット
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05439909

反応ノート

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