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Methyl iodide → Methyl 3-bromo-5-fluoro-4-methoxybenzoate

HRID 521535
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HRID 521535 반응식
[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[C:8]([F:10])[C:7]([OH:11])=[C:6]([Br:12])[CH:5]=1.[C:14](=O)([O-])[O-].[K+].[K+].IC>CC(C)=O>[CH3:1][O:2][C:3](=[O:13])[C:4]1[CH:9]=[C:8]([F:10])[C:7]([O:11][CH3:14])=[C:6]([Br:12])[CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 57467610Methyl 3-bromo-5-fluoro-4-hydroxybenzoate

생성물 1

HCID 67076673Methyl 3-bromo-5-fluoro-4-methoxybenzoate

시약·촉매·용매 1

HCID 180Acetone용매

실험 절차

6 g (24.09 mmol) of the product obtained in step 1 were dissolved in 60 ml of acetone, 10.13 g (2.270 mmol) of potassium carbonate and 6.84 g (48.18 mmol) of iodomethane were added, and the mixture was stirred for 4 days. Then is was filtered and evaporated. The resulting product (5.8 g) was used in the next step without further purification.

후처리

  1. filtrationThen is was filtered
  2. customevaporated
  3. customThe resulting product (5.8 g) was used in the next step without further purification

출처 및 근거

ORD 기록
ord-655597f546b3408f909ac54e3c6d0729
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09328071B2

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