HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1674430Generated: October 30, 2026
Pyridine → Methyl 2,2,2-trifluoroethyl carbonate
https://huagongshe.com/reaction/1674430
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 2,2,2-trifluoroethyl carbonate | HCID 17761042 | — |
Reaction Steps
2,2,2-trifluoroethanol (105 g 1.05 mol), pyridine (87 g 1.1 mol) and 300 mL of methylene chloride were combined in a 1 L 3-neck round bottom flask. The flask was equipped with an overhead stirring mechanism, thermocouple, addition funnel, cold water condenser, and a dry nitrogen bubbler. The reaction flask was kept cool using a dry ice/acetone bath to keep the temperature in the range of −20° C. to −15° C. Methylchloroformate (100 g 1.05 mol) was added via an addition funnel at such a rate that the temperature was kept in the range of −20° C. to −15° C. Once the addition of the methylchloroformate was complete the reaction mix was allowed to warm to room temperature. The reaction mix was then quenched with 100 mL water. The methylene chloride solution was separated from the water and washed with 2×100 mL of 1N HCl. The methylene chloride was removed by distillation and the product was purified using fractional distillation on a concentric tube column (b.p.=90.0° C., purity=99.7%). The structure mass was confirmed by GC/MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08003004B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-b73f13634de84c53913e6b892b1c3b00 |
|---|
| Source note | uspto-grants-2011_08 |
|---|