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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730769Generated: October 30, 2026

3,4,5-Trifluorobenzaldehyde → HCID 178505860, compound

https://huagongshe.com/reaction/730769

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrifluorobenzaldehydeHCID 2776954—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 178507663HCID 178507663—
SolventChloroformHCID 6212—
ProductHCID 178505860HCID 178505860—

Reaction Steps

NaBH(OAc)3 (211 mg, 1 mmol, Aldrich) was added to a mixture of 5-(trifluoromethyl)-2-{4-[3-(trifluoromethyl)pyridin-2-yl]piperazin-1-yl}-1H-benzimidazol-7-amine (215 mg, 0.5 mmol, Example 58) and 3,4,5-trifluoro-benzaldehyde (88 mg, 0.55 mmol, Aldrich) in chloroform (2 mL) in one portion. The reaction mixture was stirred at room temperature for 2 h and concentrated in vacuo. The residue was dissolved in EtOAc (30 mL), and washed successively with 1 N NaOH (15 mL) and brine (15 mL), dried over MgSO4, filtered, and the solvent was evaporated in vacuo. The residue was purified by silica gel chromatography, eluting with 25% EtOAc/hexane to give the title compound as a white solid. MS (ESI, pos. ion) m/z: 575 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582761B2
Source datasetuspto-grants-2009_09
ORD IDord-8543e5083038418b86f76039db565e7d
Source noteuspto-grants-2009_09