HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Lutidine → 2-((tert-Butyldimethylsilyl)oxy)ethyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Trifluoromethanesulfonate | HCID 2758875 | — |
| Reactant | 2-(Tert-butyldimethylsilyl)-ethylene glycol | HCID 13681251 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-((tert-Butyldimethylsilyl)oxy)ethyl trifluoromethanesulfonate | HCID 15678107 | — |
Reaction Steps
A solution of 2-(tert-butyldimethylsilyl)-ethylene glycol (125 mg, 0.71 mmol) and 2,6-lutidene (0.08 mL, 0.69 mmol) in 6 mL dichloromethane was cooled to −78° C. Trifluoromethanesulfonic anhydride (0.11 mL, 0.65 mmol) was added over a period of 5 min and stirring was continued for additional 15 min at −78° C. to complete the formation of the triflate. The triflate was used in situ for the reaction as described in 3.2 below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897608B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-0871dd79b7244323abdfeb90e4cf57c8 |
| Source note | uspto-grants-2011_03 |