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Iodoethane → HCID 15027468、化合物

HRID 373684
ノート
印刷プレビュー

反応式

HRID 373684 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-70db4c3c35ab41c495d01785051dff59
出典データセット
uspto-grants-1992_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05164513

反応ノート

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