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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643489Generated: October 30, 2026

Phosphoric Acid → 2-(Trifluoromethyl)pyrimidin-5-yl trifluoromethanesulfonate

https://huagongshe.com/reaction/643489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Trifluoromethyl)pyrimidin-5-olHCID 13590680—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(Trifluoromethyl)pyrimidin-5-yl trifluoromethanesulfonateHCID 8661516090%

Reaction Conditions

Temperature4 °C

Reaction Steps

Triflic anhydride (13.9 g, 85 mmol) in dry DCM (70 mL) was added slowly to an ice-cold solution of 2-(trifluoromethyl)pyrimidin-5-ol (13.9, 85 mmol) (U.S. Pat. No. 4,558,039), DIPEA (16 mL, 93 mmol) and dry DCM (260 mL) at such a rate that the temperature was kept between 4° C. and 6° C. After the addition was complete, the solution was stirred for 2.5 h at 4° C. and then allowed to warm to RT. Water (50 mL) and 1M phosphoric acid (4.5 mL) were added and the phases were washed and separated. The organic phase was washed successively with water and saturated sodium bicarbonate, dried, filtered and carefully concentrated by rotary evaporation (pressure 300-400 mbar). The dark-red oil was purified by column chromatography with EtOAc-heptanes (1:8 through 1:4) as eluent to give 22.5 g (90%) of the title product as a colourless oil that crystallised in the cold. Alternatively, the product could be purified by distillation, b.p. 75-77° C./10 mbar.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700604B2
Source datasetuspto-grants-2010_04
ORD IDord-e7764099b4474ccc8b257b799414b4ef
Source noteuspto-grants-2010_04