Tributyltin Chloride → HCID 67260270, compound

HRID 2043385Notes

Reaction equation

HRID 2043385 reaction equation
Br[C:2]1[S:6][C:5]([N:7]2[CH:11]=[CH:10][N:9]=[C:8]2[CH3:12])=[CH:4][CH:3]=1.[Li]CCCC.[CH2:18]([Sn:22](Cl)([CH2:27][CH2:28][CH2:29][CH3:30])[CH2:23][CH2:24][CH2:25][CH3:26])[CH2:19][CH2:20][CH3:21].[NH4+].[Cl-]>C1COCC1>[CH3:12][C:8]1[N:7]([C:5]2[S:6][C:2]([Sn:22]([CH2:23][CH2:24][CH2:25][CH3:26])([CH2:27][CH2:28][CH2:29][CH3:30])[CH2:18][CH2:19][CH2:20][CH3:21])=[CH:3][CH:4]=2)[CH:11]=[CH:10][N:9]=1

Participants

6

Conditions

Temperature
-78 °C

Procedure

To the solution of 1-(5-bromothiophen-2-yl)-2-methyl-1H-imidazole (2 g, 8.3 mmol) in dried THF was added dropwise n-BuLi (2.5 M in hexane, 4 mL, 10 mmol) at −78° C., the mixture was stirred at −78° C. for 30 min. A solution of tributyltin chloride (4.6 g, 0.96 mmol) in THF was added dropwise, the solution was stirred at −78° C. for 1 hour, and the reaction solution was allowed to warm to room temperature and stirred for 1 hour. The reaction solution was poured into NH4Cl aqueous solution, the mixture was extracted with EtOAc (100 mL×3). The organic layer was washed with brine, dried over Na2SO4, then concentrated under reduced pressure, and the residue was purified by column chromatography to give 2-methyl-1-(5-(tributylstannyl)thiophen-2-yl)-1H-imidazole as a yellow oil (1.2 g, yield 31.8%).

Workup

  1. stirringthe solution was stirred at −78° C. for 1 hour
  2. temperatureto warm to room temperature
  3. stirringstirred for 1 hour
  4. extractionthe mixture was extracted with EtOAc (100 mL×3)
  5. washThe organic layer was washed with brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated under reduced pressure
  8. customthe residue was purified by column chromatography

Sources & evidence

ORD record
ord-d0b745d3ec2947b3b7230697143772e8
Source dataset
uspto-grants-2013_11
Patent number
US08586624B2

Reaction notes

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