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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methyl iodide → HCID 67244819, 화합물

HRID 2425060
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HRID 2425060 반응식
[Br:1][C:2]1[CH:3]=[C:4]([CH2:7][OH:8])[O:5][CH:6]=1.[H-].[Na+].I[CH3:12]>CS(C)=O>[Br:1][C:2]1[CH:3]=[C:4]([CH2:7][O:8][CH3:12])[O:5][CH:6]=1
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참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 24758Sodium hydrideHCID 12289784(4-Bromofuran-2-yl)methanol

생성물 1

HCID 67244819HCID 67244819, 화합물

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

실험 절차

To a solution of 1.062 g (4-bromo-furan-2-yl)-methanol in 10 ml dimethylsulfoxide was added 0.288 of sodium hydride (55%) in oil and 0.56 ml of iodomethane and the reaction mixtures was stirred at room temperature for 18 h. The reaction mixture was partitioned between ethyl acetate and water. The phases were separated; the organic phase was washed with citric acid (10% in water), water, satd. sodiumbicarbonate and brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by chromatography on silica gel to yield 0.731 g of a light yellow liquid.

후처리

  1. customthe reaction mixtures
  2. customThe reaction mixture was partitioned between ethyl acetate and water
  3. customThe phases were separated
  4. washthe organic phase was washed with citric acid (10% in water), water
  5. dry with materialsodiumbicarbonate and brine, dried over magnesium sulfate
  6. customevaporated under reduced pressure
  7. customThe residue was purified by chromatography on silica gel

출처 및 근거

ORD 기록
ord-9a686c44a52e49b2a255e32bf1cbe324
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07964633B2

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