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Iodoethane → HCID 21191829, 화합물

HRID 1602117
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HRID 1602117 반응식
[H-].[Na+].[CH3:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[NH:10][C:11](=[O:14])[O:12][CH3:13].[CH2:15](I)[CH3:16]>CN(C)C=O>[CH2:15]([N:10]([C:5]1[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=1[CH3:3])[C:11](=[O:14])[O:12][CH3:13])[CH3:16]
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참가 물질

5

반응물 3

HCID 6340IodoethaneHCID 24758Sodium hydrideHCID 519038Carbamic acid, (2-methylphenyl)-, methyl ester

생성물 1

HCID 21191829HCID 21191829, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

5.1 g (0.2 mol) of sodium hydride are added a little at a time to 30 g (0.18 mol) of methyl N-(o-methylphenyl)-carbamate (Example 1a) in 200 ml of dimethylformamide. After the evolution of gas has ceased, 30 g (0.2 mol) of ethyl iodide are added drop-wise, the reaction mixture being lightly cooled in a water bath. A white solid is precipitated. After about 4 hours, the reaction mixture is diluted with water and the aqueous phase is extracted three times with ether. The organic phase is dried over MgSO4 and evaporated down. The residue is distilled. 32.5 g (0.17 mol=93%) of the title compound are obtained as a colorless oil. bp.0.5 =74° C.

후처리

  1. temperaturethe reaction mixture being lightly cooled in a water bath
  2. customA white solid is precipitated
  3. additionthe reaction mixture is diluted with water
  4. extractionthe aqueous phase is extracted three times with ether
  5. dry with materialThe organic phase is dried over MgSO4
  6. customevaporated down
  7. distillationThe residue is distilled

출처 및 근거

ORD 기록
ord-ace2df1c42eb4366a69d76c543969c5d
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05981532

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