Water → 3,4-Dimethoxyphenylethanolamine

HRID 1385902ノート

反応式

HRID 1385902 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:8]=[CH:9][C:10]=1[O:11][CH3:12])[CH:6]=[O:7].C[Si](O[C:18]#[N:19])(C)C.[H-].[Al+3].[Li+].[H-].[H-].[H-].O>C(Cl)Cl.O1CCCC1.[I-].[Zn+2].[I-]>[NH2:19][CH2:18][CH:6]([C:5]1[CH:8]=[CH:9][C:10]([O:11][CH3:12])=[C:3]([O:2][CH3:1])[CH:4]=1)[OH:7]

参加物

8

実験手順

3,4-dimethoxybenzaldehyde (2.00 g, 12.04 mM) and trimethylsilyl cyanate (1.57 g, 15.04 mM) were dissolved in dry methylene chloride (1 ml). While stirring at room temperature, zinc iodide (8.5 mg) was carefully added and the mixture was stirred for 2 hours. Next, the solution was dropwise added to a solution of lithium aluminum hydride (1.10 g, 28.88 mM) in dried tetrahydrofuran (120 ml) cooled to 0° C., then the reaction temperature was gradually warmed to room temperature and the mixture was stirred for 1 hour. Water (2 ml) was carefully added while cooling the reaction solution in an ice bath, the mixture was stirred for 1 hour, then the solution was filtered through Celite. The filtrate was dried over anhydrous magnesium sulfate, then the solvent was evaporated in vacuo to obtain a crude product (2.37 g) as a yellow solid. The crude product thus obtained had a sufficient purity even without purification, so could be used for the next reaction as it was.

後処理

  1. stirringthe mixture was stirred for 2 hours
  2. temperaturecooled to 0° C.
  3. temperaturethe reaction temperature was gradually warmed to room temperature
  4. stirringthe mixture was stirred for 1 hour
  5. temperaturewhile cooling the reaction solution in an ice bath
  6. stirringthe mixture was stirred for 1 hour
  7. filtrationthe solution was filtered through Celite
  8. dry with materialThe filtrate was dried over anhydrous magnesium sulfate
  9. customthe solvent was evaporated in vacuo
  10. customto obtain a crude product (2.37 g) as a yellow solid

出典と根拠

ORDレコード
ord-cc151d4bf090468cacdfc7271b9a259c
出典データセット
uspto-grants-2001_07
特許番号
US06265402B1

反応ノート

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