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Water → 2-[N-methyl-(4-trifluoromethoxyphenyl)-amino]ethanol

HRID 856023
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인쇄 미리보기

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HRID 856023 반응식
[CH3:1][NH:2][C:3]1[CH:8]=[CH:7][C:6]([O:9][C:10]([F:13])([F:12])[F:11])=[CH:5][CH:4]=1.Br[CH2:15][CH2:16][O:17]C1CCCCO1.C(=O)([O-])[O-].[K+].[K+].O>CN(C=O)C>[CH3:1][N:2]([C:3]1[CH:8]=[CH:7][C:6]([O:9][C:10]([F:11])([F:12])[F:13])=[CH:5][CH:4]=1)[CH2:15][CH2:16][OH:17]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 11430Potassium CarbonateHCID 866212-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 737351n-Methyl-4-(trifluoromethoxy)aniline

생성물 1

HCID 694797632-[N-methyl-(4-trifluoromethoxyphenyl)-amino]ethanol수율 54.4%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

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온도
100 °C

실험 절차

A mixture of N-methyl-(4-trifluoromethoxyphenyl)amine (4.83 g, 24.24 mmol), 2-(2-bromoethoxy)-tetrahydropyran (6.1 g, 29.03 mmol), and potassium carbonate (3.84 g, 27.76 mmol) in DMF (20 ml) was stirred at 100° C. for 5 hours. The reaction mixture was allowed to return to room temperature, poured into water, and extracted with ethyl acetate twice. The extract was washed with water twice and brine, and dried over magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride/ethyl acetate=20/1) to afford 2-[N-methyl-(4-trifluoromethoxyphenyl)-amino]ethanol (3.1 g, yield 53%) as a pale yellow oil.

후처리

  1. customto return to room temperature
  2. extractionextracted with ethyl acetate twice
  3. washThe extract was washed with water twice
  4. dry with materialbrine, and dried over magnesium sulfate
  5. filtrationAfter filtration
  6. concentrationthe filtrate was concentrated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (methylene chloride/ethyl acetate=20/1)

출처 및 근거

ORD 기록
ord-073843149b46452298e48ccbed9587f2
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07262212B2

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