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Iodoethane → HCID 20360292, 화합물

HRID 437421
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HRID 437421 반응식
[CH3:1][O:2][C:3]1[CH:11]=[C:7]([C:8]([NH2:10])=[O:9])[C:6]([OH:12])=[CH:5][CH:4]=1.I[CH2:14][CH3:15]>[Na].C(O)C>[CH2:14]([O:12][C:6]1[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:11][C:7]=1[C:8]([NH2:10])=[O:9])[CH3:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6340IodoethaneHCID 1199772-Hydroxy-5-methoxybenzamide

생성물 1

HCID 20360292HCID 20360292, 화합물수율 70.7%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 5360545Sodium용매

실험 절차

5-Methoxysalicylamide (41.8 g., 0.250 mole) was dissolved in a solution of sodium (6.37 g., 0.277 g-atom) in ethanol (250 ml.). To the resulting cooled (ice-water) solution was added iodoethane (38.9 g., 0.250 mole) over a period of 20 minutes. The reaction mixture was allowed to warm to room temperature over 0.75 hour and then was heated under reflux for 19 hours. The mixture was concentrated and the residue triturated with water. The mixture was filtered and collected solid recrystallized from acetonitrile to give 2-ethoxy-5-methoxybenzamide (34.5 g., 70.7%), m.p. 128°-130°.

후처리

  1. temperaturewas heated
  2. temperatureunder reflux for 19 hours
  3. concentrationThe mixture was concentrated
  4. customthe residue triturated with water
  5. filtrationThe mixture was filtered
  6. customcollected solid
  7. customrecrystallized from acetonitrile

출처 및 근거

ORD 기록
ord-fc8ac2d5c136432e85d91d2bb8876718
출처 데이터셋
uspto-grants-1977_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04031093

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