Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trifluoromethanesulfonic acid | HCID 62406 | — |
| Reactant | Dimethylthexylsilyl chloride | HCID 144239 | — |
| Product | TDS triflate | HCID 4080852 | — |
Reaction Steps
50 ml of trifluoromethanesulfonic acid are slowly added dropwise at room temperature under argon to 101.57 g (0.57 mol) of (1,1,2,2-tetramethyleth-1-yl)-dimethylchlorosilane. Subsequently, the mixture is heated for 8 hours at 60° C. After this time, the evolution of HCl ceases. 111 g (67% of theory) of a colourless oil of boiling point=123°-124° C./28.6 mbar are obtained by distillation. The 1H-NMR spectrum is in agreement with the structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04801719 |
|---|
| Source dataset | uspto-grants-1989_01 |
|---|
| ORD ID | ord-f80c631598144f359f57e41871a5c7fa |
|---|
| Source note | uspto-grants-1989_01 |
|---|