Trimethyltin chloride → HCID 21112930, Verbindung

HRID 1767184

Reaktionsgleichung

Reaktionsgleichung von HRID 1767184
C([Li])CCC.[Br:6][C:7]1[CH2:11][CH2:10][CH2:9][C:8]=1Br.[CH3:13][Sn:14](Cl)([CH3:16])[CH3:15]>C1COCC1>[Br:6][C:7]1[CH:11]=[CH:10][CH2:9][C:8]=1[Sn:14]([CH3:16])([CH3:15])[CH3:13]

Komponenten

5

Reaktionsbedingungen

Temperatur
-75 °C

Versuchsvorschrift

n-Butyllithium, 1.6M in hexanes, (58 mL, 92.0 mmol) in THF (50 mL) was cooled under nitrogen to −75° C. 1,2-Dibromocyclopentene (10.00 g, 44.3 mmol) in dry THF (10 mL) was added dropwise over ˜10 minutes. The mixture was stirred at −75° C. for a further 20 minutes and then allowed to reach 0° C. The reaction mixture was then re-cooled to −75° C. and trimethyltin chloride (8.85 g, 44.3 mmol) in THF (30 mL) was added, under nitrogen, over ˜10 minutes. After stirring at −75° C. for 30 minutes the reaction was allowed to reach room temperature and then stirred for 2 hours. The reaction mixture was then evaporated down to an oil and partitioned between brine and dichloromethane (100/200 mL). After shaking thoroughly, the organic layer was dried (magnesium sulphate), filtered and evaporated to give an oil. (13.15 g, ˜80% pure).

Aufarbeitung

  1. customto reach 0° C
  2. temperatureThe reaction mixture was then re-cooled to −75° C.
  3. stirringAfter stirring at −75° C. for 30 minutes the reaction
  4. customto reach room temperature
  5. stirringstirred for 2 hours
  6. customThe reaction mixture was then evaporated down to an oil
  7. custompartitioned between brine and dichloromethane (100/200 mL)
  8. stirringAfter shaking thoroughly
  9. dry with materialthe organic layer was dried (magnesium sulphate)
  10. filtrationfiltered
  11. customevaporated
  12. customto give an oil

Quellen und Nachweise

ORD-Eintrag
ord-36c0f916d7454ab6b154f8c4dd56cd69
Quelldatensatz
uspto-grants-2007_06
Patentnummer
US07232821B2

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