Reaction #833536

ord-fabce88f1d534e5eb46d76575315e462

Reaction equation

CI
methyl iodide
Ic1ccc2c(c1)Cc1ccccc1-2
2-Iodofluorene
CS(C)=O
dimethylsulfoxide
CCOCC
diethylether
[Na+].[OH-]
NaOH
CC1(C)c2ccccc2-c2ccc(I)cc21
product
Yield 88.0%
CC1(C)c2ccccc2-c2ccc(I)cc21
2-iodo-9,9-dimethyl-fluorene
Yield 88.0%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    workup.ADDITIONwas added through the septum
  2. 2
    TemperatureAfter cooling to ambient temperature the mixture
  3. 3
    Otherwas transferred to a 1 L separatory funnel
  4. 4
    OtherThe organic layer was collected
  5. 5
    Extractionthe aqueous layer was extracted with diethyl ether (4×100 mL)
  6. 6
    Dryingdried over anhydrous magnesium sulfate
  7. 7
    Otherthe solvent evaporated under vacuo

Procedure

A 500 mL round bottomed flask was charged with 21.8 g (70 mmol) 2-Iodofluorene and 1.18 g (5 mmol) benzyltriethylammonium chloride. 200 mL of dimethylsulfoxide (DMSO) was then added followed by 28 mL (50%) NaOH. The mixture was allowed to stir under nitrogen for 1 hour, before 29 g (210 mmol) methyl iodide was added through the septum. The mixture was allowed to stir at room temperature for 18 hours. After cooling to ambient temperature the mixture was transferred to a 1 L separatory funnel. 100 mL of water and 100 mL of diethylether were added to the mixture. The organic layer was collected and the aqueous layer was extracted with diethyl ether (4×100 mL). The organic fractions were combined, dried over anhydrous magnesium sulfate, and the solvent evaporated under vacuo. A flash column was then performed using hexanes as the eluent to give 21.0 g (88% yield) of the product (yellow oil).

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07393599B2uspto-grants-2008_07