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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Fluorophenol → Benzene, 1-(3-buten-1-yloxy)-4-fluoro-

HRID 2395419
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HRID 2395419 반응식
Br[CH2:2][CH2:3][CH:4]=[CH2:5].[F:6][C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[CH:9][CH:8]=1.C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[F:6][C:7]1[CH:12]=[CH:11][C:10]([O:13][CH2:5][CH2:4][CH:3]=[CH2:2])=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 97324-FluorophenolHCID 11430Potassium CarbonateHCID 21241Homoallyl bromide

생성물 1

HCID 18971814Benzene, 1-(3-buten-1-yloxy)-4-fluoro-수율 36%

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

A solution of 4-bromo-1-butene (4.0 g), 4-fluorophenol (3.0 g), potassium carbonate (3.8 g) and acetone (75 ml) was heated at reflux over 16 hours. The mixture was then concentrated in vacuo, dluted with ether, washed with water followed by 1N sodium hydroxide, dried over sodium sulfate, filtered, and concentrated in vacuo. Chromatography on a silica gel column eluting with 25% ethyl acetate-hexane afforded 1.6 g of a colorless oil.

후처리

  1. temperatureat reflux over 16 hours
  2. concentrationThe mixture was then concentrated in vacuo
  3. washwashed with water
  4. dry with materialdried over sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo
  7. washChromatography on a silica gel column eluting with 25% ethyl acetate-hexane

출처 및 근거

ORD 기록
ord-8da0142d35ed43beaa759a5b59177616
출처 데이터셋
uspto-grants-1998_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05814651

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