Tributylvinyltin → 5-Ethenyl-2-(trifluoromethyl)pyridine

HRID 2195861Notes

Reaction equation

HRID 2195861 reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]([C:8]([F:11])([F:10])[F:9])=[N:6][CH:7]=1.[CH:12]([Sn](CCCC)(CCCC)CCCC)=[CH2:13]>CN(C=O)C.C1COCC1>[F:9][C:8]([F:11])([F:10])[C:5]1[CH:4]=[CH:3][C:2]([CH:12]=[CH2:13])=[CH:7][N:6]=1

Participants

4

Conditions

Temperature
100 °C

Procedure

2 g of 5-bromo-2-(trifluoromethyl)pyridine was dissolved in DMF:THF (3:1, 12 mL). vinyltributyltin (3 g) and tetrakis (triphenylphosphine)palladium (135 mg) were added to this solution. The reaction mixture was degassed and purged with nitrogen for 5 min and then heated at 100° C. for 2 h. at which point the reaction was found complete (monitored by TLC). The reaction mixture was diluted with water and extracted with ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate and evaporated under reduced pressure (Caution: product may be volatile) and the residue was purified by SiO2 chromatography (100-200 mesh, eluent: hexane-ethyl acetate gradient). The requisite fractions were concentrated below 40° C. under reduced pressure to obtain 20.3 g of 2-(trifluoromethyl)-5-vinylpyridine as oil.

Workup

  1. customThe reaction mixture was degassed
  2. custompurged with nitrogen for 5 min
  3. additionThe reaction mixture was diluted with water
  4. extractionextracted with ethyl acetate
  5. dry with materialThe combined organic layer was dried over anhydrous sodium sulfate
  6. customevaporated under reduced pressure (Caution: product may be volatile)
  7. customthe residue was purified by SiO2 chromatography (100-200 mesh, eluent: hexane-ethyl acetate gradient)
  8. concentrationThe requisite fractions were concentrated below 40° C. under reduced pressure

Sources & evidence

ORD record
ord-0e15233ffa1c4ec9a5d35c8323689e7d
Source dataset
uspto-grants-2012_12
Patent number
US08338408B2

Reaction notes

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