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Iodoethane → HCID 15027468、化合物

HRID 1090804
ノート
印刷プレビュー

反応式

HRID 1090804 の反応式
[OH:1][C:2]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[OH:18])([CH2:9][CH2:10][CH3:11])[CH2:3][N:4]1[CH:8]=[CH:7][N:6]=[CH:5]1.[CH2:19](I)[CH3:20].[OH-].[Na+]>CN(C)C=O>[OH:1][C:2]([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[O:18][CH2:19][CH3:20])([CH2:9][CH2:10][CH3:11])[CH2:3][N:4]1[CH:8]=[CH:7][N:6]=[CH:5]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 6340IodoethaneHCID 14798Sodium HydroxideHCID 15027467HCID 15027467、化合物2 回

生成物 1

HCID 15027468HCID 15027468、化合物収率 58.1%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

34 mg of 1-[2-hydroxy-2-(2-hydroxyphenyl)pentyl]imidazole (Compound 18) was dissolved into 10 ml of dimethylformamide, and 33 mg of ethyl iodide and 10 mg of sodium hydroxide was added to this solution. The mixture was stirred at room temperature for 20 hours. The reaction mixture, after being charged into ice water, was subjected to extraction with ether. The ether layer was then washed with water, followed by drying over anhydrous magnesium sulfate. The extract thus obtained was purified by means of silica gel column chromatography (eluent: methylene chloride) to produce 22 mg of the title compound at a yield of 58%.

後処理

  1. additionwas added to this solution
  2. extractionwas subjected to extraction with ether
  3. washThe ether layer was then washed with water
  4. dry with materialby drying over anhydrous magnesium sulfate
  5. extractionThe extract thus
  6. customobtained
  7. customwas purified by means of silica gel column chromatography (eluent: methylene chloride)

出典と根拠

ORDレコード
ord-9d646430d3484bfc8bf378d752f01c99
出典データセット
uspto-grants-1992_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05082948

反応ノート

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このページの内容参加物実験手順後処理出典と根拠反応ノート