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Methyl iodide → HCID 10205143, 화합물

HRID 2180926
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HRID 2180926 반응식
[CH3:1][I:2].[N:3]1([CH2:10][CH2:11][CH:12]([C:19]2[CH:24]=[C:23]([CH3:25])[CH:22]=[CH:21][C:20]=2[OH:26])[C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1>C(Cl)Cl>[I-:2].[OH:26][C:20]1[CH:21]=[CH:22][C:23]([CH3:25])=[CH:24][C:19]=1[CH:12]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[CH2:11][CH2:10][N+:3]1([CH3:1])[CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6328Methyl iodideHCID 69315919HCID 69315919, 화합물

생성물 1

HCID 10205143HCID 10205143, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Methyl iodide (10 equivalents) was added to a solution of the free base 2-(3-azepan-1-yl-1-phenylpropyl)-4-methylphenol of Example 30 (0.3 g, 1.02 mmol) in CH2Cl2 (2 mL). The reaction mixture was stirred overnight at room temperature. The solution was concentrated to initiate precipitation of the resulting quaternary ammonium salt. The white precipitate was filtered out, washed with diethyl ether and dried under vacuum to give a quaternized salt.

후처리

concentration
The solution was concentrated
  • customprecipitation of the resulting quaternary ammonium salt
  • filtrationThe white precipitate was filtered out
  • washwashed with diethyl ether
  • customdried under vacuum
  • customto give a quaternized salt
  • 출처 및 근거

    ORD 기록
    ord-bacb85878a884113aafa73681a845555
    출처 데이터셋
    uspto-grants-2005_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06890920B2

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