Pentane → HCID 19437716, compound

HRID 2255832Notes

Reaction equation

HRID 2255832 reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]2[C:9]3[CH:10]=[CH:11][C:12]([CH2:14][O:15][Si:16]([C:19]([CH3:22])([CH3:21])[CH3:20])([CH3:18])[CH3:17])=[CH:13][C:8]=3[O:7][C:6]=2[CH:23]=1.C([Li])(C)(C)C.CCCCC.[CH3:34][Sn:35](Cl)([CH3:37])[CH3:36]>C1COCC1.C(Cl)Cl.CCOCC>[CH3:34][Sn:35]([CH3:37])([CH3:36])[C:2]1[CH:3]=[CH:4][C:5]2[C:9]3[CH:10]=[CH:11][C:12]([CH2:14][O:15][Si:16]([C:19]([CH3:22])([CH3:21])[CH3:20])([CH3:18])[CH3:17])=[CH:13][C:8]=3[O:7][C:6]=2[CH:23]=1

Participants

8

Procedure

To a solution of the dibenzofuran 4 (995 mg, 2.5 mmol) in anhydrous THF (25 mL) at -78° C. under a nitrogen atmosphere was added a 1.5M t-butyllithium in pentane solution (3.0 mL, 5.25 mmol). The resulting yellow solution was stirred for 100 min., then trimethyltin chloride (548 mg, 2.75 mmol) was added as a solid. The mixture was allowed to warm to ambient temperature and then stirred for 3 hours. The reaction mixture was then poured into ether and the organic solution was washed with water (3 times) and then with brine. The organic solution was then dried with magnesium sulfate, filtered and concentrated under vacuum. Flash chromatography of the residue (silica gel, 10% methylene chloride in hexanes) provided 815 mg of the stannane 23 (68% yield) as a crystalline solid.

Workup

  1. stirringstirred for 3 hours
  2. washthe organic solution was washed with water (3 times)
  3. dry with materialThe organic solution was then dried with magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated under vacuum

Sources & evidence

ORD record
ord-a0f6afad498e49dd851802ee8ddf2760
Source dataset
uspto-grants-1993_08
Patent number
US05240920

Reaction notes

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