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Hydrochloric Acid → 3-{[3-(Dimethylamino)propyl](methyl)amino}propan-1-ol

HRID 1388207
ノート
印刷プレビュー

反応式

HRID 1388207 の反応式
[C:1]([O:5]CC)(=O)[CH:2]=[CH2:3].[CH3:8][N:9]([CH3:15])[CH2:10][CH2:11][CH2:12][NH:13][CH3:14].[H-].[H-].[H-].[H-].[Li+].[Al+3].Cl>C(OCC)(=O)C.CCOCC>[CH3:8][N:9]([CH3:15])[CH2:10][CH2:11][CH2:12][N:13]([CH3:14])[CH2:3][CH2:2][CH2:1][OH:5]
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

7

反応物 4

HCID 313Hydrochloric AcidHCID 8821Ethyl AcrylateHCID 783021,3-Propanediamine, N1,N1,N3-trimethyl-HCID 21226445Aluminium lithium hydride

生成物 1

HCID 127217913-{[3-(Dimethylamino)propyl](methyl)amino}propan-1-ol

試薬・触媒・溶媒 2

HCID 3283Diethyl Ether溶媒2 回
HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

Under stirring, 15 g. ethyl acrylate was added to 11.6 g. N,N,N'-trimethyl-propane-1,3-diamine. Stirring was continued 8 hours at room temperature and the mixture was then heated to 80° C. for 16 hours before stripping the solvent in vacuo. The residue was dissolved in 75 ml. ether and added to a slurry of 2.1 g. LiAlH4 in 100 ml. of ether. This mixture was refluxed 2 hours. After cooling, ethyl acetate and then aqueous HCl were added and the mixture was stirred one hour. The clear, two-phase system was separated. The organic layer was dried over MgSO4, filtered, stripped of solvent, and the residue was distilled at 70°-75° C./0.4 mm, producing pure N,N,N'-trimethyl-N'-(3-hydroxypropyl)propane-1,3-diamine.

後処理

  1. stirringStirring
  2. dissolutionThe residue was dissolved in 75 ml
  3. temperatureThis mixture was refluxed 2 hours
  4. temperatureAfter cooling
  5. stirringthe mixture was stirred one hour
  6. customThe clear, two-phase system was separated
  7. dry with materialThe organic layer was dried over MgSO4
  8. filtrationfiltered
  9. distillationthe residue was distilled at 70°-75° C./0.4 mm

出典と根拠

ORDレコード
ord-03671d1fa0b34600b628256628200f41
出典データセット
uspto-grants-1984_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04430455

反応ノート

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