HuagongsheHuagongshe Chemistry Print Report · For research reference only
Neopentyl alcohol → 2,2-Dimethylpropyl trifluoromethanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Neopentyl alcohol | HCID 6404 | — |
| Reactant | 2,6-Lutidine | HCID 7937 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,2-Dimethylpropyl trifluoromethanesulfonate | HCID 15696281 | 72% |
Reaction Steps
Add trifluoromethanesulphonic anhydride (1.12 mL, 6.8 mmol) to a solution of neopentylalcohol (0.5 g, 5.7 mmol) and 2,6-lutidine (0.7 mL, 6.8 mmol) in dichloromethane (10 mL) at −78° C. and stir for 1 hour. Add water to quench the reaction, separate the organic layer and extract the aqueous layer with dichloromethane. Combine the organic layers, dry (magnesium sulfate), filter, concentrate and purify (silica gel chromatography, eluting with 1:4 hexane:dichloromethane) to give the desired compound as an oil (0.9 g, 72% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07745438B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-6975154842644f7fbddb9e327f2bcaee |
| Source note | uspto-grants-2010_06 |