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

HRID 1502048
Notes
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Reaction equation

HRID 1502048 reaction equation
[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]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

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

Product 1

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

Reagents, catalysts & solvents 1

HCID 62406Trifluoromethanesulfonic acidSolvent

Procedure

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.

On this pageParticipantsProcedureWorkupSources & evidenceReaction notes

Workup

  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

Sources & evidence

ORD record
ord-01a8dcf545634e22ad91bb6a890da91e
Source dataset
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US09206199B2

Reaction notes

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