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Sodium Hydroxide → 8-Hydroxy-5,6,7,8-tetrahydroquinoline

HRID 481760
ノート
印刷プレビュー

反応式

HRID 481760 の反応式
C([O:4][CH:5]1[C:14]2[N:13]=[CH:12][CH:11]=[CH:10][C:9]=2[CH2:8][CH2:7][CH2:6]1)(=O)C.[OH-].[Na+]>CO.O>[OH:4][CH:5]1[C:14]2[N:13]=[CH:12][CH:11]=[CH:10][C:9]=2[CH2:8][CH2:7][CH2:6]1
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 122262495,6,7,8-Tetrahydroquinolin-8-yl acetate

生成物 1

HCID 118159398-Hydroxy-5,6,7,8-tetrahydroquinoline収率 102.5%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒

実験手順

To 10 g of 8-acetoxy-5,6,7,8-tetrahydroquinoline in 30 mL of methanol was added 30 mL of 30% sodium hydroxide in water. The mixture was heated to reflux for 2 min and the methanol was removed in vacuo. The residual organic product was extracted with chloroform. The chloroform extracts were dried over sodium sulfate and evaporation of the solvent gave 8 g of product as an oil, characterized by its NMR.

後処理

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 2 min
  3. customthe methanol was removed in vacuo
  4. extractionThe residual organic product was extracted with chloroform
  5. dry with materialThe chloroform extracts were dried over sodium sulfate and evaporation of the solvent

出典と根拠

ORDレコード
ord-0092b06f89b94ed58699b8e316af2ebc
出典データセット
uspto-grants-1998_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05789587

反応ノート

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