Sulfuric Acid → 2-Methylbenzenesulfonic acid hydrate
Reaction equation
[C:1]1([CH3:7])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[S:8](=O)(=[O:11])([OH:10])[OH:9].Cl[SiH](Cl)Cl>>[OH2:9].[C:1]1([CH3:7])[C:6]([S:8]([OH:11])(=[O:10])=[O:9])=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
Procedure
Toluenesulfonic acid monohydrate was prepared by dripping 6 moles toluene over a period of 1 hour into a mixture of 3.75 moles sulfuric acid and 2.25 moles fuming sulfuric acid at a mixture temperature of 45° C. to 60° C. and then ageing for an additional 30 minutes at 45° C. Into this product was then dripped the mixture of 1 mole trichlorosilane and 6.6 moles toluene over a period of 5 hours at 30° C. followed by ageing for 30 minutes at 45° C. After cooling and layer separation, the toluenesulfonic acid layer (lower layer) was removed. In order to remove the acid present in the upper layer, it was washed with suitable quantities of sulfuric acid/water (50/50 weight ratio), then sulfuric acid/water (25/75 weight ratio), and finally water. The water was then completely eliminated by azeotropic drying for 1 hour to afford a toluene solution. Removal of the toluene from this toluene solution by reduced pressure (vacuum pump) at 60° C. gave hydrogen silsesquioxane resin A. This hydrogen silsesquioxane resin A had a number-average molecular weight (Mn) of 1,650, and the value of its weight-average molecular weight/number-average molecular weight ratio (Mw /Mn) was 19.4.
Workup
- customof 1 hour
- customat a mixture temperature of 45° C. to 60° C.
- waitby ageing for 30 minutes at 45° C
- temperatureAfter cooling
- customlayer separation
- customthe toluenesulfonic acid layer (lower layer) was removed
- customIn order to remove the acid present in the upper layer, it
- washwas washed with suitable quantities of sulfuric acid/water (50/50 weight ratio)
- customby azeotropic drying for 1 hour
- customto afford a toluene solution
- customRemoval of the toluene from this toluene solution by reduced pressure (vacuum pump) at 60° C.
Sources & evidence
- ORD record
- ord-9a0bdbcd560f4a56bc594078efb2ae8a
- Source dataset
- uspto-grants-1994_12
- Patent number
- US05370903
Reaction notes
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