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Iodoethane → HCID 23134613, 화합물

HRID 1048630
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HRID 1048630 반응식
[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]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 795792-Methyl-3-nitrophenol

생성물 1

HCID 23134613HCID 23134613, 화합물수율 100.7%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

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.

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후처리

  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

출처 및 근거

ORD 기록
ord-45624fadc49d46e9aa387dbc6f610bda
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09380782B2

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