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4-Methoxy-alpha-methylbenzenepropanamine → HCID 12850096, 화합물

HRID 1614741
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반응식

HRID 1614741 반응식
[CH3:1][C:2]1[CH:10]=[CH:9][C:5]([CH:6]2[O:8][CH2:7]2)=[CH:4][C:3]=1[S:11][CH3:12].[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][CH2:22][CH:23]([NH2:25])[CH3:24])=[CH:17][CH:16]=1>C1C=CC=CC=1>[CH3:13][O:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][CH2:22][CH:23]([NH:25][CH2:7][CH:6]([C:5]2[CH:9]=[CH:10][C:2]([CH3:1])=[C:3]([S:11][CH3:12])[CH:4]=2)[OH:8])[CH3:24])=[CH:17][CH:16]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4102024-Methoxy-alpha-methylbenzenepropanamineHCID 12850095HCID 12850095, 화합물

생성물 1

HCID 12850096HCID 12850096, 화합물수율 29.2%

시약·촉매·용매 1

HCID 241Benzene용매

반응 조건

온도
115 °C

실험 절차

A mixture of 6 g of 4-methyl-3-methylthiostyrene oxide and 7 g of 3-(4-methoxyphenyl)-1-methylpropylamine was heated to 115° C. for 3 hours. After the reaction was over, the reaction mixture was dissolved in 100 ml of benzene and after washing twice each time with 200 ml of water, the benzene layer was purified by a silica gel column chromatography (eluate: a mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio) to provide 3.5 g of amorphous α-{[3-(4-methoxyphenyl)-1-methylpropylamino]methyl}-4-methyl-3-methylthiobenzenemethanol.

후처리

  1. washafter washing twice each time with 200 ml of water
  2. customthe benzene layer was purified by a silica gel column chromatography (eluate
  3. additiona mixture of benzene, ethyl acetate, and methanol (4:3:1 by volume ratio)

출처 및 근거

ORD 기록
ord-eebc6ba1663b45e2aa58c09b544997f8
출처 데이터셋
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05198587

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