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Thionyl Chloride → 1-chloro-2-[N-(3,4-dimethoxyphenethyl)-N-methylamino]ethane

HRID 1106881
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HRID 1106881 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:13]=[CH:14][C:15]=1[O:16][CH3:17])[CH2:6][CH2:7][N:8]([CH2:10][CH2:11]O)[CH3:9].S(Cl)([Cl:20])=O>C(Cl)Cl>[Cl:20][CH2:11][CH2:10][N:8]([CH2:7][CH2:6][C:5]1[CH:13]=[CH:14][C:15]([O:16][CH3:17])=[C:3]([O:2][CH3:1])[CH:4]=1)[CH3:9]
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 144073182-((3,4-Dimethoxyphenethyl)(methyl)amino)ethanol

생성물 1

HCID 136051471-chloro-2-[N-(3,4-dimethoxyphenethyl)-N-methylamino]ethane

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

The 2-[N-(3,4-dimethoxyphenethyl)-N-methylamino]ethanol as produced in Example 4-(1) in an amount of 2 g (8.36 mmol) was added to methylene chloride (20 ml) and thionyl chloride (0.91 ml, 12.54 mmol) was slowly added dropwise at room temperature, followed by stirring for 24 h. Thereafter, the reaction mixture was subjected to extraction with methylene chloride and washed with a saturated solution of sodium bicarbonate, followed by drying with anhydrous magnesium sulfate and evaporation of the solvent to yield the end compound 1-chloro-2-[N-(3,4-dimethoxyphenethyl)-N-methylamino]ethane (2.15 g)

후처리

  1. additionwas slowly added dropwise at room temperature
  2. extractionThereafter, the reaction mixture was subjected to extraction with methylene chloride
  3. washwashed with a saturated solution of sodium bicarbonate
  4. dry with materialby drying with anhydrous magnesium sulfate and evaporation of the solvent

출처 및 근거

ORD 기록
ord-0c700e8f71294c2bbba4d65b7ee808af
출처 데이터셋
uspto-grants-2000_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06057358

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