Pentane → HCID 19437716, compound

HRID 1494280Notes

Reaction equation

HRID 1494280 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

Reactant 4

HCID 8003PentaneHCID 14016Trimethyltin chlorideHCID 19432448HCID 19432448, compoundHCID 178418306HCID 178418306, compound

Product 1

HCID 19437716HCID 19437716, compoundYield 68.6%

Reagents, catalysts & solvents 3

HCID 3283Diethyl EtherSolventHCID 6344DichloromethaneSolventHCID 8028TetrahydrofuranSolvent

Procedure

To a solution of the dibenzofuran 10 (995 mg, 2.5 mmol) in anhydrous THF (25 mL) at -78° C. under a nitrogen atmosphere was added a 1.7M t-butyllithium in pentane solution (3.0 mL, 5.1 mmol). The resulting yellow solution was stirred from 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 vaccum. Flash chromatography of the residue (silica gel, 10% methylene chloride in hexanes) provided 815 mg of the stannane 316 (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 vaccum

Sources & evidence

ORD record
ord-47a4077acfa341c3b603c29e59f516bd
Source dataset
uspto-grants-1991_06
Patent number
US05025008

Reaction notes

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