Methanol → Dibutyl(difluoro)stannane

HRID 1193949Notes

Reaction equation

HRID 1193949 reaction equation
[CH2:1]([Sn:5](Cl)(Cl)[CH2:6][CH2:7][CH2:8][CH3:9])[CH2:2][CH2:3][CH3:4].CO.O.[F-:15].[F-:16].[NH4+].[NH4+]>>[CH2:1]([Sn:5]([F:16])([F:15])[CH2:6][CH2:7][CH2:8][CH3:9])[CH2:2][CH2:3][CH3:4]

Participants

5

Procedure

Advantageously, dibutyl tin chloride and an ammonium difluoride are reacted to form a dibutyl tin difluoride precipitate. Dibutyl tin dichloride (DBTCl) is solubilized in an alcohol, preferably methanol, in a first reaction vessel. In a second such vessel, ammonium difluoride (NH4F, HF) is dissolved in a solvent which is preferably water. The contents of one reaction vessel are poured into the other and, on contact of the two solutions, a dibutyl tin difluoride precipitate is formed. The mixture is stirred to enhance the contact between the two solutions and to maximize the yield of precipitate. The resulting precipitate is recovered, drained, washed with water, washed with a solvent such as acetone to eliminate any remaining water and dried.

Workup

  1. customThe contents of one reaction vessel
  2. additionare poured into the other and, on contact of the two solutions

Sources & evidence

ORD record
ord-13e9f547d0cd499483408f97bf469f7b
Source dataset
uspto-grants-1989_03
Patent number
US04812332

Reaction notes

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