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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972168Generated: October 31, 2026

Trifluoroacetic acid → HCID 67486234, compound

https://huagongshe.com/reaction/1972168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67486552HCID 67486552—
SolventDichloromethaneHCID 6344—
ProductHCID 67486234HCID 6748623499.7%

Reaction Steps

tert-Butyl 4-(2-methylpyridin-3-yloxy)pyridin-2-ylcarbamate (5.5 g, 18.3 mmol) was diluted in dichloromethane (20 mL). Trifluoroacetic acid (20 mL) was added and the reaction was stirred for 3 hours at ambient temperature. The reaction was concentrated, and saturated sodium bicarbonate solution was added to the residue. The aqueous layer was extracted with ethyl acetate and organic layer was dried and concentrated to give the title compound (3.67 g, 99% yield) as light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431713B2
Source datasetuspto-grants-2013_04
ORD IDord-1c047d5afb304f97a3f7cad3b29c416e
Source noteuspto-grants-2013_04