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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ethanol → HCID 91882220, 화합물

HRID 513222
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인쇄 미리보기

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HRID 513222 반응식
[Br:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([I:11])[CH:3]=1.[CH2:12](O)[CH3:13]>S(Cl)(Cl)=O>[CH2:12]([O:7][C:6](=[O:8])[C:5]1[CH:9]=[CH:10][C:2]([Br:1])=[CH:3][C:4]=1[I:11])[CH3:13]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 702EthanolHCID 190915044-Bromo-2-iodobenzoic acid

생성물 1

HCID 91882220HCID 91882220, 화합물

시약·촉매·용매 1

HCID 24386Thionyl Chloride용매

반응 조건

온도
0 °C

실험 절차

4-Bromo-2-iodo-benzoic acid (4.0 g; 12.24 mmol) is stirred in thionyl chloride (8.0 ml) under reflux for 1 hour. The reaction mixture is evaporated under reduced pressure and taken up immediately in 20 ml methylene dichloride and cooled down to 0° C. Ethanol (20.0 ml; 342.96 mmol) is added and stirred for 1 hour at ambient temperature. The ethanol is evaporated and the residue taken up in methylene dichloride and extracted with saturated NaHCO3 solution. The organic layer is separated, dried over MgSO4 and evaporated to dryness.

후처리

  1. temperatureunder reflux for 1 hour
  2. customThe reaction mixture is evaporated under reduced pressure
  3. customThe ethanol is evaporated
  4. extractionextracted with saturated NaHCO3 solution
  5. customThe organic layer is separated
  6. dry with materialdried over MgSO4
  7. customevaporated to dryness

출처 및 근거

ORD 기록
ord-17cdf5ccef394070bdbbe23256e05bb4
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102684B2

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