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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054253Generated: October 25, 2026

4,4,4-Trifluoro-1-(4-trifluoromethylphenyl)-1,3-butanedione → HCID 11441169, compound

https://huagongshe.com/reaction/2054253

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4,4-Trifluoro-1-(4-trifluoromethylphenyl)-1,3-butanedioneHCID 10859020—
ReactantHCID 178509259HCID 178509259—
ProductHCID 11441169HCID 1144116946%

Reaction Steps

Reaction of 1-(4-trifluoromethyl-phenyl)-4,4,4-trifluoro-butane-1,3-dione (142 mg, 0.5 mmol), prepared from commercially available 4-trifluoromethyl-acetophenone according to general procedure A, and 3-amino-4-(4-pyridinyl)-pyrazole [CAS No. 216661-87-9; prepared from 4-cyanomethyl-pyridine as described in Bioorg. Med. Chem. Lett. 12 (2002) 3537-3541] (80 mg, 0.5 mmol) according to general procedure B yielded the title compound as a yellow solid (93 mg, 46%). MS (ISP) 409.2 [(M+H)+]; mp 261° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329662B2
Source datasetuspto-grants-2008_02
ORD IDord-bc526c9ed9564da68aab8e71cb79d64f
Source noteuspto-grants-2008_02