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Methyl sulfate, sodium salt → 1,3-Dimethyl-2-chloroimidazolidinium methylsulfate

HRID 2116867
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HRID 2116867 반응식
[CH3:1][N:2]1[CH2:6][CH2:5][N:4]([CH3:7])[C:3]1(Cl)[Cl:8].[CH3:10][O:11][S:12]([O-:15])(=[O:14])=[O:13].[Na+]>C(#N)C>[CH3:10][O:11][S:12]([O-:15])(=[O:14])=[O:13].[CH3:1][NH+:2]1[CH2:6][CH2:5][N:4]([CH3:7])[CH:3]1[Cl:8]
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참가 물질

4

반응물 2

HCID 2735086Methyl sulfate, sodium saltHCID 127556762,2-Dichloro-1,3-dimethylimidazolidine

생성물 1

HCID 866130351,3-Dimethyl-2-chloroimidazolidinium methylsulfate수율 94.2%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

3.00 g (17.75 mmol) of 1,3-dimethyl-2,2-dichloroimidazolidine and 2.38 g (17.75 mmol) of sodium methylsulfate are mixed with 20 ml of dry acetonitrile. The reaction mixture is stirred for 5 hours at room temperature, and the precipitate NaCl is filtered off. The solvent is distilled off, and the residue is dried for 1 hour under a reduced pressure of 7 Pa and at 50° C., giving 4.09 g of 1,3-dimethyl-2-chloroimidazolidinium methylsulfate as a viscous material, corresponding to a yield of 94.2%.

후처리

  1. filtrationthe precipitate NaCl is filtered off
  2. distillationThe solvent is distilled off
  3. customthe residue is dried for 1 hour under a reduced pressure of 7 Pa and at 50° C.

출처 및 근거

ORD 기록
ord-8a66758521a44f5ab15978a0d5deb961
출처 데이터셋
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07439395B2

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