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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557419Generated: October 31, 2026

Potassium tert-butoxide → HCID 66991689, compound

https://huagongshe.com/reaction/557419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-Amino-4,4,4-trifluorobut-2-enenitrileHCID 53401096—
ReactantHCID 66991397HCID 66991397—
SolventIsopropanolHCID 3776—
ProductHCID 66991689HCID 66991689—

Reaction Steps

A solution of 345 mg (1.06 mmol) of cyclobutyl 2-[(2-methyl-4-oxo-4H-chromen-8-yl)methylene]-3-oxobutanoate in 30 ml of 2-propanol is mixed with 143.85 mg (1.06 mmol) of 3-amino-4,4,4-trifluorobut-2-enenitrile [preparation in analogy to K. Krespan, J. Org. Chem. 34, 42-45 (1969)] and 17.8 mg (0.16 mmol) of potassium tert-butoxide and stirred under reflux for 12 h. After cooling, the mixture is concentrated. The residue is purified on an Analogix cartridge (F12M) (mobile phase: cyclohexane/ethyl acetate 2:1). After concentration of the product fractions, the residue is crystallized from diethyl ether. 50.9 mg (10.8% of theory) of the title compound are obtained as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058447B2
Source datasetuspto-grants-2011_11
ORD IDord-1fe1b42621a84426aa513a0a74400b77
Source noteuspto-grants-2011_11