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Hydrochloric Acid → [(2,4-Dimethoxyphenyl)methyl](methyl)amine

HRID 1426695
ノート
印刷プレビュー

反応式

HRID 1426695 の反応式
[CH3:1][O:2][C:3]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:4]=1[CH:5]=O.[CH3:13][NH2:14].[BH4-].[Na+].Cl>CO>[CH3:1][O:2][C:3]1[CH:10]=[C:9]([O:11][CH3:12])[CH:8]=[CH:7][C:4]=1[CH2:5][NH:14][CH3:13]
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 6329MethylamineHCID 691752,4-DimethoxybenzaldehydeHCID 4311764Sodium borohydride

生成物 1

HCID 2416536[(2,4-Dimethoxyphenyl)methyl](methyl)amine収率 81%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

2,4-Dimethoxybenzaldehyde (5.0 g) was dissolved in methanol (60 mL), and a 40% methanol solution (9.3 mL) of methylamine was added at room temperature. The mixture was stirred at room temperature for 1 hr, and sodium borohydride (1.37 g) was added by small portions under ice-cooling. The mixture was stirred at room temperature for 3 hr, treated with 1 mol/L hydrochloric acid under ice-cooling, and methanol was evaporated under reduced pressure. The residue was diluted with ethyl acetate, basified with saturated aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent: hexane:ethyl acetate=4:1→2:1) to give the title compound as a colorless oil (yield 4.41 g, 81%).

後処理

  1. temperaturecooling
  2. stirringThe mixture was stirred at room temperature for 3 hr
  3. temperaturecooling
  4. custommethanol was evaporated under reduced pressure
  5. additionThe residue was diluted with ethyl acetate
  6. extractionextracted with ethyl acetate
  7. washThe extract was washed with saturated brine
  8. dry with materialdried over anhydrous sodium sulfate
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by basic silica gel column chromatography (eluent: hexane:ethyl acetate=4:1→2:1)

出典と根拠

ORDレコード
ord-ebcde0bc413b4de382768e90dc2c129d
出典データセット
uspto-grants-2015_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08933105B2

反応ノート

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