HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1669662Generated: November 1, 2026
Potassium Phosphate, Tribasic → 2-(Trifluoromethyl)pyrimidin-5-yl trifluoromethanesulfonate
https://huagongshe.com/reaction/1669662
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 2-(Trifluoromethyl)pyrimidin-5-ol | HCID 13590680 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(Trifluoromethyl)pyrimidin-5-yl trifluoromethanesulfonate | HCID 86615160 | 93% |
Reaction Steps
Triflic anhydride (1.01 mL, 6.0 mmol) was added dropwise to a stirred mixture of 2-(trifluoromethyl)pyrimidin-5-ol (prepared according to U.S. Pat. No. 4,558,039) (0.82 g, 5.0 mmol), toluene (10 mL) and aqueous tripotassium phosphate (30% by weight, 10 mL) at ice-bath temperature (Frantz et al., Organic Letters, 2002, 4(26), 4717-4718). When the addition was complete the ice-bath was taken away and the solution was stirred at ambient temperature for 30 minutes. The clear phases were separated and the organic layer was washed with water, then brine. Drying of the organic phase over anhydrous sodium sulfate, filtration and concentration by rotary evaporation at room temperature afforded 2-(trifluoromethyl)-pyrimidine-5-yl trifluoromethanesulfonate as a colourless oil (1.38 g, 93%). B.p. 75-77° C. (10 mbar).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07989620B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-6a632ed410874d589aae6c578154a61e |
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| Source note | uspto-grants-2011_08 |
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