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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592385Generated: October 30, 2026

Trifluoroacetic anhydride → HCID 67272592, compound

https://huagongshe.com/reaction/1592385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 67272534HCID 67272534—
SolventDichloromethaneHCID 6344—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 67272592HCID 6727259248%

Reaction Steps

To a solution of 2,3-dimethyl-5-trifluoromethyl-pyridine 1-oxide (0.620 g, 3.24 mmol) in CH2Cl2 (20 mL) was added TFAA (1.36 g, 6.48 mmol) at room temperature. After the mixture was stirred at room temperature for 3 h, brine (5 mL) and K2CO3 (20 mL) were added. The mixture was stirred at room temperature for 1 h and then extracted with CH2Cl2 (3×20 mL). The extracts were combined and dried over Na2SO4. After filtration the solvent was removed, and the residue was purified on silica gel column (4:1, CH2Cl2/Et2O), affording (2,3-dimethyl-5-trifluoromethyl-pyridin-2-yl)-methanol as a pale yellow oil (0.300 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291631B2
Source datasetuspto-grants-2007_11
ORD IDord-c747f50be03241db818ee6e0aa3676f4
Source noteuspto-grants-2007_11