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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735147Generated: October 30, 2026

2,2,3,3,3-Pentafluoropropylamine → 4-[3,4-Dioxo-2-(2,2,3,3,3-pentafluoro-propylamino)cyclobut-1-enylamino]-benzonitrile

https://huagongshe.com/reaction/1735147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,3,3,3-PentafluoropropylamineHCID 79002—
Reactant4-[(2-Ethoxy-3,4-dioxocyclobut-1-en-1-yl)amino]benzonitrileHCID 10824058—
SolventEthanolHCID 702—
Product4-[3,4-Dioxo-2-(2,2,3,3,3-pentafluoro-propylamino)cyclobut-1-enylamino]-benzonitrileHCID 1943697571%

Reaction Steps

4-(3,4-Dioxo-2-ethoxy-cyclobut-1-enylamino)-benzonitrile (1 g, 4.1 mmol) and 2,2,3,3,3-pentafluoropropylamine (3 mL) in ethanol were refluxed for 24 hours. The reaction mixture was filtered and the resulting solid was triturated with diethyl ether to give 1.0 g (71% ) of 4-[3,4-dioxo-2-(2,2,3,3,3-pentafluoro-propylamino)-cyclobut-1-enylamino]-benzonitrile as a yellow solid: mp 272°-275° C. (dec); 1H NMR (DMSO-d6): δ 10.15 (br s, 1H), 8.19 (br s, 1H), 7.81 (d, 2H), 7.79 (d, 2H), 4.54 (dt, 2H). IR (KBr): 3185. 2239, 1804, 1672, 1608, 1565, 1548 cm-1 ; MS (m/z) 346([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05536731
Source datasetuspto-grants-1996_07
ORD IDord-e92cc53205124ba98e63cebf60e49210
Source noteuspto-grants-1996_07