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Methyl iodide → 2,3,4,5-tetrahydro-alpha-methyl-1-methyl-1H-1-benzazepine-7-methanol

HRID 2247965
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반응식

HRID 2247965 반응식
[Mg].[CH3:2]I.[CH3:4][N:5]1[C:11]2[CH:12]=[CH:13][C:14]([CH:16]=[O:17])=[CH:15][C:10]=2[CH2:9][CH2:8][CH2:7][CH2:6]1.[Cl-].[NH4+]>CCOCC>[CH3:2][CH:16]([C:14]1[CH:13]=[CH:12][C:11]2[N:5]([CH3:4])[CH2:6][CH2:7][CH2:8][CH2:9][C:10]=2[CH:15]=1)[OH:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6328Methyl iodideHCID 25517Ammonium ChlorideHCID 5462224MagnesiumHCID 19935434HCID 19935434, 화합물

생성물 1

HCID 199353992,3,4,5-tetrahydro-alpha-methyl-1-methyl-1H-1-benzazepine-7-methanol

시약·촉매·용매 1

HCID 3283Diethyl Ether용매2회

실험 절차

The Grignard reagent was prepared from 1.04 g of magnesium shavings and 2.30 ml of methyl iodide under argon in 40 ml of absolute ether. To this Grignard solution was slowly added dropwise at room temperature a solution of 4.38 g of 2,3,4,5-tetrahydro-1-methyl-1H-1-benzazepine-7-carboxaldehyde in 10 ml of ether. The reaction mixture was stirred for 2 hours. Thereafter, the mixture was hydrolyzed with saturated ammonium chloride solution, extracted with ether, washed with water and dried. After evaporation, there were obtained 4.47 g of 2,3,4,5-tetrahydro-α-methyl-1-methyl-1H-1-benzazepine-7-methanol as a yellow oil.

후처리

  1. extractionextracted with ether
  2. washwashed with water
  3. customdried
  4. customAfter evaporation

출처 및 근거

ORD 기록
ord-02e5f6806d574c8ea1573e221a900c31
출처 데이터셋
uspto-grants-1991_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05037825

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