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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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p-Bromoacetophenone → 2-(4-Bromophenyl)propan-2-ol

HRID 76160
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인쇄 미리보기

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HRID 76160 반응식
[CH3:1][C:2]([C:4]1[CH:9]=[CH:8][C:7]([Br:10])=[CH:6][CH:5]=1)=[O:3].[CH3:11][Mg+].[Br-]>C(OCC)C>[Br:10][C:7]1[CH:8]=[CH:9][C:4]([C:2]([OH:3])([CH3:11])[CH3:1])=[CH:5][CH:6]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7466p-BromoacetophenoneHCID 178418689HCID 178418689, 화합물

생성물 1

HCID 126819202-(4-Bromophenyl)propan-2-ol

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

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온도
0 °C

실험 절차

20.0 g (100 mmol) 4-bromoacetophenone are added to 300 mL diethylether and cooled down to 0° C. 35.2 mL MeMgBr (3M in diethylether) are added by a dropping funnel. Cooling is removed and the mixture is stirred at r.t. over night. The reaction quenched by careful addition of 150 mL sat. aq. NH4Cl solution and 150 mL water. The resulting mixture is stirred for 20 min. The layers are separated and the org. layer is washed with water (2×), dried with MgSO4 and the solvent is removed in vacuo.

후처리

  1. temperatureCooling
  2. customis removed
  3. customThe reaction quenched by careful addition of 150 mL sat. aq. NH4Cl solution and 150 mL water
  4. stirringThe resulting mixture is stirred for 20 min
  5. customThe layers are separated
  6. washlayer is washed with water (2×)
  7. dry with materialdried with MgSO4
  8. customthe solvent is removed in vacuo

출처 및 근거

ORD 기록
ord-bc092db86e90497488c901f7343b86e1
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08835472B2

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