Methyl iodide → Acetylcholine Iodide

HRID 1275370

反応式

HRID 1275370 の反応式
[CH3:1][N:2]([CH2:4][CH2:5][OH:6])[CH3:3].[3H][CH2:8][C:9](ON1C(=O)C2=CC=CC=C2C1=O)=[O:10].[CH3:23][I:24]>C(#N)C>[I-:24].[C:9]([O:6][CH2:5][CH2:4][N+:2]([CH3:23])([CH3:3])[CH3:1])(=[O:10])[CH3:8]

参加物

5

反応条件

温度
75 °C

実験手順

N,N-Dimethylaminoethanol (4 μL, 0.04 mmole) was dissolved in dry acetonitrile (0.25 mL) and was placed in a reaction vessel connected to the vacuum line. N-tritioacetoxyphthalimide (0.04 mmole, specific activity 13 Ci/mmole) in dry acetonitrile (0.8 mL) was then added through the side-arm of the reaction vessel. The mixture was heated at 75° C. for 2 hours under N2, then brought to room temperature and methyl iodide (20 μL) was injected. The mixture was stirred for 1 hour. The solvent and excess of methyl iodide was evaporated under vacuum. Deuteriated water (0.5 mL) was added and removed. D2O (1 mL) was then added to the residue and filtered and the product was analyzed by 1H and 3H NMR spectroscopy.

後処理

  1. customwas placed in a reaction vessel
  2. custombrought to room temperature
  3. customThe solvent and excess of methyl iodide was evaporated under vacuum
  4. additionDeuteriated water (0.5 mL) was added
  5. customremoved
  6. additionD2O (1 mL) was then added to the residue
  7. filtrationfiltered

出典と根拠

ORDレコード
ord-9a70f0f9c217492ba5b74e4a4ac0990c
出典データセット
uspto-grants-2000_12
特許番号
US06160128

関連ノート

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