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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Sodium Iodide → 3-Methoxyphenethyl iodide

HRID 568780
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HRID 568780 반응식
CS(O[CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([O:14][CH3:15])[CH:9]=1)(=O)=O.[I-:16].[Na+]>CC(C)=O>[CH3:15][O:14][C:10]1[CH:9]=[C:8]([CH:13]=[CH:12][CH:11]=1)[CH2:7][CH2:6][I:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5238Sodium IodideHCID 130615423-Methoxyphenethyl mesylate

생성물 1

HCID 109014123-Methoxyphenethyl iodide수율 87.9%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

To a flask under argon was added 14.6 g (0.0634 mole) 2-(3-methoxyphenyl)ethyl methanesulfonate in 400 ml of acetone and 36.5 g (0.243 mole) of sodium iodide. The reaction mixture was refluxed for 2.5 hr. The acetone was evaporated in vacuo and the residue dissolved in ether. The ether was washed with water, sodium bicarbonate, sodium thiosulfate, water and brine, dried over MgSO4, and evaporated in vacuo to give a light green oil. Distillation in a Kugelrohr apparatus gave 14.6 g of the desired product as a clear oil.

후처리

  1. temperatureThe reaction mixture was refluxed for 2.5 hr
  2. customThe acetone was evaporated in vacuo
  3. dissolutionthe residue dissolved in ether
  4. washThe ether was washed with water, sodium bicarbonate, sodium thiosulfate, water and brine
  5. dry with materialdried over MgSO4
  6. customevaporated in vacuo
  7. customto give a light green oil
  8. distillationDistillation in a Kugelrohr apparatus

출처 및 근거

ORD 기록
ord-2e268c1b31fb4351950561eda9728d02
출처 데이터셋
uspto-grants-1988_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04729994

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