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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667565Generated: October 29, 2026

3,5-Bis(trifluoromethyl)benzaldehyde → HCID 178517826, compound

https://huagongshe.com/reaction/1667565

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Bis(trifluoromethyl)benzaldehydeHCID 136247—
ReactantHCID 178514360HCID 178514360—
CatalystAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductHCID 178517826HCID 17851782672%

Reaction Steps

To a solution of 4-chloro-6-hydrazino-[1,3,5]triazin-2-ol (0.13 g, 0.0008 mol) and 3,5-bis(trifluoromethyl)benz aldehyde (0.39 g, 0.0016 mol) in abs. EtOH (10 mL), was added 1 drop of acetic acid. The reaction mixture was refluxed for 5 hours. The reaction mixture was cooling to room temperature and concentrated to remove solvent. The resulting residue was solidified by EtOAc to give red solid 0.21 g, in 72% yield, mp: 258.3° C. 1H NMR (DMSO-d6) δ 11.15 (s, 1H), 8.97 (s, 1H), 8.54 (s, 1H), 7.59 (s, 1H), 7.30 (s, 2H). 13C NMR (DMSO-d6) δ 179.0, 160.2, 149.8, 148.8, 128.3, 127.6, 125.4, 124.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044241B2
Source datasetuspto-grants-2011_10
ORD IDord-dcaca714097c4b0f8ae1c9f6f7372da5
Source noteuspto-grants-2011_10