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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633875Generated: October 31, 2026

Pyridine → HCID 18680108, compound

https://huagongshe.com/reaction/1633875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,2,2-TrifluoroethanolHCID 6409—
ReactantPotassium CarbonateHCID 11430—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 18680150HCID 18680150—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 18680108HCID 18680108—

Reaction Steps

A solution of 2,2,2-trifluoroethanol (0.88 mL, 12 mmol) and pyridine (0.9 mL, 12 mmol)in dichloromethane (10 mL) at 0° C. was treated dropwise with trifluoromethanesulfonic anhydride (2.0 mL, 12 mmol), stirred for 15 minutes, warmed to room temperature, and stirred for 18 hours. The solution (0.7 mL, 0.84 mmol) was added dropwise to a mixture of Example 20A (150 mg, 0.41 mmol) and K2CO3 (172 mg, 1.2mmol) in DMF (1.1 mL), stirred for 24 hours, treated with water, and extracted with dichloromethane. The combined extracts were washed with brine, dried (MgSO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel using 10% ethyl acetate/hexanes to provide the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06504031B1
Source datasetuspto-grants-2003_01
ORD IDord-ca40a671a38442b59c09015c1e61b727
Source noteuspto-grants-2003_01