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Formaldehyde → (2-Methyl-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

HRID 2081497
ノート
印刷プレビュー

反応式

HRID 2081497 の反応式
[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH:3]([CH2:11][OH:12])[NH:2]1.C=O.[Na].[C:16](=O)([O-])[O-].[K+].[K+]>C(O)=O>[CH3:16][N:2]1[CH:3]([CH2:11][OH:12])[CH2:4][C:5]2[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH2:1]1
参加物反応条件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 712FormaldehydeHCID 11430Potassium CarbonateHCID 3752277(1,2,3,4-Tetrahydro-isoquinolin-3-yl)-methanolHCID 5360545Sodium

生成物 1

HCID 589740(2-Methyl-1,2,3,4-tetrahydroisoquinolin-3-yl)methanol

試薬・触媒・溶媒 1

HCID 284Formic Acid溶媒

反応条件

温度
140 °C

実験手順

In a sealed tube, a mixture of 1.80 g of 1,2,3,4-tetrahydro-3-isoquinolinemethanol, 1.69 g of 90% formic acid and 1.04 g of 35% formalin was heated at 140° C. for 16 hours. The reaction solution was cooled and then made alkaline by addition of 10% aqueous sodium solution. Subsequently, potassium carbonate was added to the solution and a precipitated oil was extracted with chloroform. The extract was dried over anhydrous sodium sulfate and placed under reduced pressure to remove the solvent. There was obtained 1.95 g of 2-methyl-1,2,3,4-tetrahydro-3-isoquinolinemethanol.

後処理

  1. temperatureThe reaction solution was cooled
  2. extractiona precipitated oil was extracted with chloroform
  3. dry with materialThe extract was dried over anhydrous sodium sulfate
  4. customto remove the solvent

出典と根拠

ORDレコード
ord-5a05dda084ce464681427f416f392cdf
出典データセット
uspto-grants-1993_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05183811

反応ノート

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