Lithium Bromide → N-(4(5-bromopent-1-yn-1-yl)phenyl)-2,2,2-trifluoroacetamide

HRID 385260Notes

Reaction equation

HRID 385260 reaction equation
Cl[CH2:2][CH2:3][CH2:4][C:5]#[C:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][C:14](=[O:19])[C:15]([F:18])([F:17])[F:16])=[CH:9][CH:8]=1.[Br-:20].[Li+]>CCC(=O)CC>[Br:20][CH2:2][CH2:3][CH2:4][C:5]#[C:6][C:7]1[CH:12]=[CH:11][C:10]([NH:13][C:14](=[O:19])[C:15]([F:18])([F:17])[F:16])=[CH:9][CH:8]=1

Participants

4

Reactant 2

HCID 82050Lithium Bromide2×HCID 57516939N-(4-(5-chloropent-1-ynyl)phenyl)-2,2,2-trifluoroacetamide

Product 1

HCID 56923688N-(4(5-bromopent-1-yn-1-yl)phenyl)-2,2,2-trifluoroacetamide

Reagents, catalysts & solvents 1

HCID 7288Ethyl ketoneSolvent

Procedure

A solution of Intermediate 25 (approximately 10 mmol) in 3-pentanone (200 mL) was treated with lithium bromide (10 eq, 100 mmol). The mixture was heated to reflux for 16 hours, followed by concentration to dryness under reduced pressure. The residue was taken up in ethyl acetate and washed with water. The concentrated organic phase was taken up again in 3-pentanone (200 mL) and heated to reflux for four hours in the presence of lithium bromide (10 eq, 100 mmol). The mixture was concentrated to dryness under reduced pressure. The residue was partitioned between ethyl acetate and water. The organic phase was washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, filtered, and concentrated to dryness under reduced pressure. The crude product was purified via automated flash silica gel chromatography, using a 40 g SiliSep flash column (hexanes/ethyl acetate). Concentration of the desired fractions under reduced pressure provided the title compound as an off-white solid. ES/MS calcd. for C13H12BrF3NO+ 334.0. found m/z=334.1 (M+H)+.

Workup

  1. temperatureThe mixture was heated
  2. temperatureto reflux for 16 hours
  3. concentrationfollowed by concentration to dryness under reduced pressure
  4. washwashed with water
  5. temperatureheated
  6. concentrationThe mixture was concentrated to dryness under reduced pressure
  7. customThe residue was partitioned between ethyl acetate and water
  8. washThe organic phase was washed with saturated aqueous sodium chloride solution
  9. dry with materialdried over anhydrous magnesium sulfate
  10. filtrationfiltered
  11. concentrationconcentrated to dryness under reduced pressure
  12. customThe crude product was purified via automated flash silica gel chromatography

Sources & evidence

ORD record
ord-e136e5aa10ab49daad3600b6e97cea77
Source dataset
uspto-grants-2013_02
Patent number
US08367829B2

Reaction notes

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