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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1747026Generated: November 2, 2026

Trifluoroacetic anhydride → HCID 59479126, compound

https://huagongshe.com/reaction/1747026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 59478794HCID 59478794—
SolventDimethylformamideHCID 6228—
ProductHCID 59479126HCID 59479126—

Reaction Steps

To a solution of 1891 mg of (6-methyl-1-oxidopyridin-3-yl)methyl benzoate in 38 ml of DMF was added 11 ml of trifluoroacetic anhydride, followed by stirring at room temperature overnight. After evaporating trifluoroacetic anhydride under reduced pressure, a saturated aqueous sodium hydrogen carbonate solution was added thereto, followed by extraction with chloroform. The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent:chloroform-methanol) to obtain 3.675 g of [6-(hydroxymethyl)pyridin-3-yl]methyl benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150541B2
Source datasetuspto-grants-2015_10
ORD IDord-1cfe30c20ad74fca90533b72912848b9
Source noteuspto-grants-2015_10