Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantMethyl chloroformateHCID 6586—
SolventDichloromethaneHCID 6344—
ProductMethyl 2,2,2-trifluoroethyl carbonateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003004B2
Source datasetuspto-grants-2011_08
ORD IDord-b73f13634de84c53913e6b892b1c3b00
Source noteuspto-grants-2011_08