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Hydrochloric Acid → HCID 10488443、化合物

HRID 482286
ノート
印刷プレビュー

反応式

HRID 482286 の反応式
C[O:2][C:3]([C:5]1[CH:6]=[C:7]2[C:11](=[CH:12][C:13]=1[C:14]([O:16]C)=[O:15])[NH:10][CH:9]=[CH:8]2)=[O:4].C(O)C.[OH-].[Na+].Cl>O>[NH:10]1[C:11]2[C:7](=[CH:6][C:5]([C:3]([OH:4])=[O:2])=[C:13]([C:14]([OH:16])=[O:15])[CH:12]=2)[CH:8]=[CH:9]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 313Hydrochloric AcidHCID 702EthanolHCID 14798Sodium HydroxideHCID 105137935,6-Dimethoxycarbonylindole

生成物 1

HCID 10488443HCID 10488443、化合物収率 86.5%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a stirred solution of the dimethyl ester produced in step d (1.14 g, 4.9 mmol) in a 5:1 mixture of ethanol:water (12 ml) was added solid sodium hydroxide (0.49 g, 12.4 mmol). The solution was stirred at a gentle reflux for 3 h. The solution was acidifed on cooling to pH2 with hydrochloric acid and then evaporated. The residue was azeotroped with ethanol and then toluene and dried under vacuum. The residue was then extracted with hot acetone (5×20 ml) and the combined extracts were evaporated to leave the title compound (870 mg).

後処理

  1. temperaturea gentle reflux for 3 h
  2. customevaporated
  3. customThe residue was azeotroped with ethanol
  4. dry with materialtoluene and dried under vacuum
  5. extractionThe residue was then extracted with hot acetone (5×20 ml)
  6. customthe combined extracts were evaporated

出典と根拠

ORDレコード
ord-5096d8217ba94830a0dcabd268827c1b
出典データセット
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05795907

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