Dibutyltin oxide → Acetic acid,2,2'-[(dibutylstannylene)bis(thio)]bis-, 1,1'-diisooctyl ester

HRID 1086909Notes

Reaction equation

HRID 1086909 reaction equation
[CH2:1]([Sn:5](=O)[CH2:6][CH2:7][CH2:8][CH3:9])[CH2:2][CH2:3][CH3:4].[CH2:11]([CH:19]([SH:23])[C:20]([O-:22])=[O:21])[CH2:12][CH2:13][CH2:14][CH2:15][CH:16]([CH3:18])[CH3:17]>>[CH2:11]([CH:19]([SH:23])[C:20]([O-:22])=[O:21])[CH2:12][CH2:13][CH2:14][CH2:15][CH:16]([CH3:17])[CH3:18].[CH2:11]([CH:19]([SH:23])[C:20]([O-:22])=[O:21])[CH2:12][CH2:13][CH2:14][CH2:15][CH:16]([CH3:17])[CH3:18].[CH2:1]([Sn+2:5][CH2:6][CH2:7][CH2:8][CH3:9])[CH2:2][CH2:3][CH3:4]

Participants

3

Conditions

Temperature
110 °C

Procedure

A suitable reactor was charged with 248.7 grams (1.0 mole) of dibutyltin oxide and 425.4 grams (2.05 moles) of isooctylthioglycolate of commercial purity. The reaction mixture was heated under vacuum, with agitation, to about 110° C. while distilling off water of reaction. On cooling and filtering, 656.1 grams of dibutyltin bis(isooctylthioglycolate) was obtained as an oily liquid.

Workup

  1. distillationwhile distilling off
  2. customwater of reaction
  3. temperatureOn cooling
  4. filtrationfiltering

Sources & evidence

ORD record
ord-61bb24366e584ffa8ba8a957788f3b68
Source dataset
uspto-grants-1991_07
Patent number
US05032634

Reaction notes

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