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Iodoethane → HCID 23134613、化合物

HRID 1048630
ノート
印刷プレビュー

反応式

HRID 1048630 の反応式
[CH3:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[CH:4][C:3]=1[OH:11].I[CH2:13][CH3:14].C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[CH2:13]([O:11][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]([N+:8]([O-:10])=[O:9])[C:2]=1[CH3:1])[CH3:14]
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 11430Potassium CarbonateHCID 795792-Methyl-3-nitrophenol

生成物 1

HCID 23134613HCID 23134613、化合物収率 100.7%

試薬・触媒・溶媒 1

HCID 180Acetone溶媒

実験手順

A mixture of 2-methyl-3-nitrophenol 33.5 g, iodoethane 41 g and potassium carbonate 90 g in acetone 400 mL was stirred with heating under reflux for ten hours. The mixtures were cooled to room temperature and filtered and the resulting filtrates were concentrated. The resulting mixtures were extracted with ethyl acetate and the organic layers were washed with water and saturated saline, and were dried over anhydrous magnesium sulfate and were then concentrated under reduced pressure. The resulting residues were subjected to a silica gel column chromatography to give 1-ethoxy-2-methyl-3-nitrobenzene 39.9 g.

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

後処理

  1. temperaturewith heating
  2. temperatureunder reflux for ten hours
  3. filtrationfiltered
  4. concentrationthe resulting filtrates were concentrated
  5. extractionThe resulting mixtures were extracted with ethyl acetate
  6. washthe organic layers were washed with water and saturated saline
  7. dry with materialwere dried over anhydrous magnesium sulfate
  8. concentrationwere then concentrated under reduced pressure

出典と根拠

ORDレコード
ord-45624fadc49d46e9aa387dbc6f610bda
出典データセット
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09380782B2

反応ノート

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