1,1-Dibromoethane → Tributyl-(4-ethylphenyl)stannane

HRID 550020

Reaction equation

HRID 550020 reaction equation
[Mg].BrC(Br)C.Br[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH3:14])=[CH:9][CH:8]=1.[CH2:15]([Sn:19](Cl)([CH2:24][CH2:25][CH2:26][CH3:27])[CH2:20][CH2:21][CH2:22][CH3:23])[CH2:16][CH2:17][CH3:18].[F-].[K+]>O1CCCC1.C(OCC)(=O)C>[CH2:24]([Sn:19]([CH2:15][CH2:16][CH2:17][CH3:18])([CH2:20][CH2:21][CH2:22][CH3:23])[C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH3:14])=[CH:9][CH:8]=1)[CH2:25][CH2:26][CH3:27]

Participants

8

Procedure

To a solution of magnesium (896 mg) in tetrahydrofuran (20 ml) was added dibromoethan (0.1 ml), and the mixture was stirred at room temperature for 15 minutes. Thereto was added dropwise a solution of 1-bromo-4-ethylbenzene (5.7 g) in tetrahydrofuran (20 ml), and subsequently, the mixture was stirred at room temperature for one hour. The reaction mixture was cooled to −78° C., and thereto was added dropwise tributyltin chloride (9.49 g). The mixture was stirred at the same temperature for 30 minutes, and then at room temperature for one hour. To the reaction mixture were added 10% aqueous potassium fluoride solution and ethyl acetate, and the mixture was stirred at room temperature for 30 minutes. Insoluble materials were filtered off. The organic layer of the filtrate was washed with water and brine successively, and dried over sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by alumina column chromatography (hexane) to give the desired tri-n-butyl(4-ethylphenyl)tin (10.7 g) as colorless oil. EI-Mass m/Z 337 (M-Bu).

Workup

  1. stirringsubsequently, the mixture was stirred at room temperature for one hour
  2. temperatureThe reaction mixture was cooled to −78° C.
  3. stirringThe mixture was stirred at the same temperature for 30 minutes
  4. waitat room temperature for one hour
  5. stirringthe mixture was stirred at room temperature for 30 minutes
  6. filtrationInsoluble materials were filtered off
  7. washThe organic layer of the filtrate was washed with water and brine successively
  8. dry with materialdried over sodium sulfate
  9. customThe solvent was evaporated under reduced pressure
  10. customthe residue was purified by alumina column chromatography (hexane)

Sources & evidence

ORD record
ord-b5edb5ae1c5e4f3a816d90afd537ab9f
Source dataset
uspto-grants-2011_05
Patent number
US07943788B2

Linked notes

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