HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonic Acid → 2-Isopropyl-3-(2,2,2-trifluoroethoxy)pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-[(1-Methylethyl)thio]-3-pyridinamine | HCID 18676416 | — |
| Product | 2-Isopropyl-3-(2,2,2-trifluoroethoxy)pyridine | HCID 18676418 | — |
Reaction Steps
A reactor vessel is charged with 3-amino-2-isopropylthiopyridine (3.0 g, 18 mmol), 2,2,2-trifluoroethanol (21 g, 210 mmol), and methanesulfonic acid (1.7 g, 18 mmol). The solution is heated to the range 65° C. to 70° C. and then t-butylnitrite (2.2 g of a 90% solution, 19 mmol) is added drop-wise to the vessel while maintaining the temperature at 65° C. to 70° C. After nitrogen evolution ceases, the solution is cooled, neutralized with aqueous saturated sodium bicarbonate solution and then extracted with MTBE. The solvent is removed by evaporation to obtain 2-isopropyl-3-(2,2,2-trifluoroethoxy)pyridine as a crude oil (4.22 g, crude yield 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06710180B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-80543af066384dcbad32e639f945787c |
| Source note | uspto-grants-2004_03 |