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N-bromobutanimide → 3-Bromo-2-chloro-6-fluorobenzonitrile

HRID 1502048
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HRID 1502048 반응식
[Cl:1][C:2]1[CH:9]=[CH:8][CH:7]=[C:6]([F:10])[C:3]=1[C:4]#[N:5].C1C(=O)N([Br:18])C(=O)C1>OS(C(F)(F)F)(=O)=O>[Br:18][C:9]1[C:2]([Cl:1])=[C:3]([C:6]([F:10])=[CH:7][CH:8]=1)[C:4]#[N:5]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 67184N-bromobutanimideHCID 695872-Chloro-6-fluorobenzonitrile

생성물 1

HCID 712393913-Bromo-2-chloro-6-fluorobenzonitrile

시약·촉매·용매 1

HCID 62406Trifluoromethanesulfonic acid용매

실험 절차

2-Chloro-6-fluorobenzonitrile (15.6 g, 100 mmol) was dissolved in triflic acid (75 mL) at 0° C., then NBS (17.8 g, 100 mmol) was added. The reaction was warmed up to room temperature and stirred overnight. The reaction mixture was poured into ice and extracted with DCM (2×). DCM layers were washed with NaHCO3 and brine. The DCM was dried over Na2SO4 then filtered and concentrated. The product was purified by chromatography through a 330 g ISCO Redi-Sep column with 10-20% ethyl acetate/hexane solvent system to yield 3-bromo-2-chloro-6-fluorobenzonitrile.

후처리

  1. additionThe reaction mixture was poured into ice
  2. extractionextracted with DCM (2×)
  3. washDCM layers were washed with NaHCO3 and brine
  4. dry with materialThe DCM was dried over Na2SO4
  5. filtrationthen filtered
  6. concentrationconcentrated
  7. customThe product was purified by chromatography through a 330 g ISCO Redi-Sep column with 10-20% ethyl acetate/hexane solvent system

출처 및 근거

ORD 기록
ord-01a8dcf545634e22ad91bb6a890da91e
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09206199B2

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