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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390749Generated: October 28, 2026

3,5-Bis(trifluoromethyl)benzyl bromide → HCID 58966545, compound

https://huagongshe.com/reaction/390749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Bis(trifluoromethyl)benzyl bromideHCID 122573—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86614959HCID 86614959—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58966545HCID 5896654580.3%

Reaction Steps

To a flask charged with (5-Bromo-pyrazin-2-yl)-[2-(2-methyl-1-morpholin-4-yl-propyl)-5-trifluoromethyl-benzyl]-amine (94 mg, 0.198 mmol) was added THF (2 mL) followed by potassium t-butoxide (28 mg, 0.249 mmol). After 4 minutes, 3,5-bis(trifluoromethyl)benzyl bromide (0.05 mL; 0.272 mol) was added. The mixture was stirred at room temperature for 2 hours. The reaction mixture was quenched with water and diluted with ethyl acetate. The mixture was washed with 2N HCl. The aqueous layer was basified with 1N NaOH and extracted with ethyl acetate (2×). The organic layers were combined, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography (silica gel) (eluting with 10-40% ethyl acetate in hexanes) to afford the title compound (111 mg, 0.159 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383660B2
Source datasetuspto-grants-2013_02
ORD IDord-26d54f958b204ceaa29b70b27c3c7740
Source noteuspto-grants-2013_02