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Methyl iodide → HCID 53760271, 화합물

HRID 342748
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HRID 342748 반응식
[CH3:1][C:2]([NH:8][C:9](=[O:18])[C:10]1[CH:15]=[C:14]([Cl:16])[CH:13]=[C:12]([Cl:17])[CH:11]=1)([CH3:7])[C:3]([CH2:5][OH:6])=[O:4].[CH3:19]I>[Ag]=O>[CH3:7][C:2]([NH:8][C:9](=[O:18])[C:10]1[CH:15]=[C:14]([Cl:16])[CH:13]=[C:12]([Cl:17])[CH:11]=1)([CH3:1])[C:3]([CH2:5][O:6][CH3:19])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6328Methyl iodideHCID 54349857HCID 54349857, 화합물

생성물 1

HCID 53760271HCID 53760271, 화합물

시약·촉매·용매 1

HCID 92152Silver(II) oxide촉매2회

실험 절차

Methyl iodide (30 ml) and freshly prepared silver oxide (0.77 gm, 0.003 m) were added to N-(1',1'-dimethyl-3'-hydroxyacetonyl)-3,5-dichlorobenzamide (0.08 gm, 0.003 m) (Example 45) and the reaction mixture was refluxed for about 10 hours. Then fresh silver oxide (0.7 gm) was added and the mixture was refluxed for another 2 hours. The inorganic salts were removed by filtration, the filter cake was washed with ether and the solvents were stripped off to obtain 0.5 gm of product after recrystallization from ethylacetate and hexane.

후처리

  1. temperaturethe reaction mixture was refluxed for about 10 hours
  2. temperaturethe mixture was refluxed for another 2 hours
  3. customThe inorganic salts were removed by filtration
  4. washthe filter cake was washed with ether

출처 및 근거

ORD 기록
ord-6c3a4b686c524347a531e68437628fe1
출처 데이터셋
uspto-grants-1999_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05859063

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