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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870982Generated: November 1, 2026

Trifluoroacetic acid → Trifluoroacetic acid

https://huagongshe.com/reaction/870982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86695962HCID 86695962—
SolventDichloromethaneHCID 6344—
ProductTrifluoroacetic acidHCID 642245%
ProductHCID 136378616HCID 136378616—

Reaction Steps

To a stirred solution of N-(7-fluoro-8-((4-methoxybenzyl)oxy)-5H-chromeno[3,4-c]pyridin-2-yl)acetamide (150 mg, 0.380 mmol) in dichloromethane (5 mL) was added TFA (0.059 mL, 0.761 mmol) at room temperature and the reaction mixture was stirred at rt for 2 h. After the completion of reaction the volatiles were removed under reduced pressure. The residue was washed with diethyl ether (7 mL) and stirred for 5 min. The solid was collected by vacuum filtration and dried under vacuum to yield N-(7-fluoro-8-hydroxy-5H-chromeno[3,4-c]pyridin-2-yl)acetamide, TFA (70 mg, 0.170 mmol, 45% yield) as a white solid. LCMS (ESI) m/e 275.0 [(M+H)+, calcd for C14H12FN2O3 275.1]; LC/MS retention time (Method E): tR=2.0 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969564B2
Source datasetuspto-grants-2015_03
ORD IDord-3ac6d46c88dd4fd3b9a862df5409e03e
Source noteuspto-grants-2015_03