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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1011338Generated: November 2, 2026

Trifluoroacetic anhydride → HCID 58478791, compound

https://huagongshe.com/reaction/1011338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantHCID 67314368HCID 67314368—
SolventDichloromethaneHCID 6344—
ProductHCID 58478791HCID 5847879157.3%

Reaction Steps

A solution of 2-methyl-7H-furo[3,4-b]pyridin-5-one N-oxide (122 mg, 0.74 mmol) in dichloromethane (2 mL) is heated at reflux. Trifluoroacetic anhydride (1.5 mL, 10 mmol) is added dropwise and heating is continued for approximately 30 min. The reaction mixture is cooled and concentrated. The residue is treated with methanol (3 mL) and triethylamine (2 mL) and stirred until no starting material remained. The reaction mixture is concentrated and the residue is purified by chromatography (silica gel). The product containing fractions are concentrated to give the title compound (70 mg, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977351B2
Source datasetuspto-grants-2011_07
ORD IDord-e28a1d04c6804074a0036250ab475997
Source noteuspto-grants-2011_07