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

HRID 1030430
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HRID 1030430 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

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

생성물 1

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

시약·촉매·용매 2

HCID 241Benzene
용매
HCID 962Water용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-d9c72a3d8deb4c689e8213fe6637da30
출처 데이터셋
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05104888

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