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Dimethylformamide → 6-Ethoxy-2,5,7,8-tetramethyl-2-(4-nitrophenoxymethyl)chroman

HRID 1030430
ノート
印刷プレビュー

反応式

HRID 1030430 の反応式
[H-].[Na+].[OH:3][C:4]1[C:5]([CH3:28])=[C:6]2[C:11](=[C:12]([CH3:15])[C:13]=1[CH3:14])[O:10][C:9]([CH3:27])([CH2:16][O:17][C:18]1[CH:23]=[CH:22][C:21]([N+:24]([O-:26])=[O:25])=[CH:20][CH:19]=1)[CH2:8][CH2:7]2.CN(C)C=O.[CH2:34](I)[CH3:35]>O.C1C=CC=CC=1>[CH2:34]([O:3][C:4]1[C:5]([CH3:28])=[C:6]2[C:11](=[C:12]([CH3:15])[C:13]=1[CH3:14])[O:10][C:9]([CH3:27])([CH2:16][O:17][C:18]1[CH:23]=[CH:22][C:21]([N+:24]([O-:26])=[O:25])=[CH:20][CH:19]=1)[CH2:8][CH2:7]2)[CH3:35]
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 6228DimethylformamideHCID 6340IodoethaneHCID 24758Sodium hydrideHCID 134888696-Hydroxy-2,5,7,8-tetramethyl-2-(4-nitrophenoxymethyl)chroman

生成物 1

HCID 198221956-Ethoxy-2,5,7,8-tetramethyl-2-(4-nitrophenoxymethyl)chroman

試薬・触媒・溶媒 2

HCID 241Benzene
溶媒
HCID 962Water溶媒

実験手順

1.6 g of a 55% w/w suspension of sodium hydride in mineral oil was added to a mixture of 11 g of 6-hydroxy-2,5,7,8-tetramethyl-2-(4-nitrophenoxymethyl)chroman and 100 ml of dimethylformamide, and the reaction mixture was stirred for 1 hour at room temperature. Then a mixture of 5.7 g of ethyl iodide and 5 ml of benzene was added dropwise, whilst ice-cooling, and the reaction mixture was stirred for 2 hours at room temperature. The reaction mixture was then poured into water and extracted with benzene. This extract was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled from the extract under reduced pressure, and the residue was purified by silica gel column chromatography eluted with a 3:7 by volume mixture of cyclohexane and benzene, to give the title compound.

後処理

  1. additionwas added dropwise, whilst ice-
  2. temperaturecooling
  3. stirringthe reaction mixture was stirred for 2 hours at room temperature
  4. extractionextracted with benzene
  5. washThis extract was washed with water
  6. dry with materialdried over anhydrous sodium sulfate
  7. distillationThe solvent was distilled from the
  8. extractionextract under reduced pressure
  9. customthe residue was purified by silica gel column chromatography
  10. washeluted with a 3:7 by volume mixture of cyclohexane and benzene

出典と根拠

ORDレコード
ord-d9c72a3d8deb4c689e8213fe6637da30
出典データセット
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05104888

反応ノート

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