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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Hydrochloric Acid → 1-(2-Bromo-4-fluorophenyl)-2,2-difluoroethan-1-one

HRID 558125
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반응식

HRID 558125 반응식
[Li]CCCC.[Br:6][C:7]1[CH:12]=[C:11]([F:13])[CH:10]=[CH:9][C:8]=1I.[F:15][CH:16]([F:22])[C:17](OCC)=[O:18].Cl>C1COCC1>[Br:6][C:7]1[CH:12]=[C:11]([F:13])[CH:10]=[CH:9][C:8]=1[C:17](=[O:18])[CH:16]([F:22])[F:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 9961Ethyl difluoroacetateHCID 27733722-Bromo-4-fluoro-1-iodobenzeneHCID 178418339Butyllithium

생성물 1

HCID 574450751-(2-Bromo-4-fluorophenyl)-2,2-difluoroethan-1-one수율 64%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Add n-BuLi (8.86 mL, 14.18 mmol) slowly to a solution of 2-bromo-4-fluoro-1-iodobenzene (4.27 g, 14.2 mmol) in THF (50 mL) at −100° C. over 15 min under N2. Stir the solution for 30 min. Add ethyl difluoroacetate (2.81 mL, 26.9 mmol) and stir for 3 h. Add an HCl (50 mL, 2 N) solution and warm the solution up to RT. Separate the organic layer, dry the organic layer over magnesium sulfate, and remove the solvent. Purify the residue by column chromatography (hexane:ethyl acetate/10:1) to give the title compound (2.3 g, 64%). MS (GC) m/z 252 [M]+.

후처리

  1. customSeparate the organic layer
  2. dry with materialdry the organic layer over magnesium sulfate
  3. customremove the solvent
  4. customPurify the residue by column chromatography (hexane:ethyl acetate/10:1)

출처 및 근거

ORD 기록
ord-2da8265ffca44b6193a090cd59854996
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063035B2

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