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Methyl iodide → 5-(3,4-Dimethoxyphenyl)-3-methyl-1,3-oxazolidin-2-one

HRID 2052561
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HRID 2052561 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]2[O:15][C:14](=[O:16])[NH:13][CH2:12]2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[H-].[Na+].[CH3:19]I>CN(C)C=O>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]2[O:15][C:14](=[O:16])[N:13]([CH3:19])[CH2:12]2)[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 30506615-(3,4-Dimethoxyphenyl)-4,5-dihydro-1,3-oxazol-2-ol

생성물 1

HCID 124381175-(3,4-Dimethoxyphenyl)-3-methyl-1,3-oxazolidin-2-one수율 60%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

10 mmol of 5-(3,4-dimethoxyphenyl)-2oxazolidinone is dissolved in 20 ml. of absolute dimethylformamide and combined with 11 mmol of sodium hydride. The mixture is then stirred for 40 minutes at 40°. After cooling, 20 mmol of methyl iodide in 5 ml. of dimethylformamide is added dropwise and thereafter the reaction mixture is agitated for 6 hours at 50°. After the dimethylformamide has been removed by evaporation, the mixture is taken up in chloroform and then washed first with a small amount of water and then with saturated sodium chloride solution, dried, filtered, and concentrated. The residue is chromatographed over 60 g. of silica gel with chloroform/methanol (96:4) as the eluent. Recrystallization from ethanol produces a 60% yield of 5-(3,4-dimethoxyphenyl)-3-methyl-2-oxazolidinone, m.p. 132°-133°.

후처리

  1. temperatureAfter cooling
  2. stirringthe reaction mixture is agitated for 6 hours at 50°
  3. customAfter the dimethylformamide has been removed by evaporation
  4. washwashed first with a small amount of water
  5. dry with materialwith saturated sodium chloride solution, dried
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe residue is chromatographed over 60 g
  9. customRecrystallization from ethanol

출처 및 근거

ORD 기록
ord-8fee6c1ae4444a55b8f3443d449d707d
출처 데이터셋
uspto-grants-1980_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04186129

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