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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 621511Generated: November 2, 2026

Potassium Carbonate → HCID 14074120, compound

https://huagongshe.com/reaction/621511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-(trifluoromethyl)pyridineHCID 92342—
Reactant1-(4-Hydroxy-3,5-dimethylphenyl)piperazine dihydrobromideHCID 21243172—
SolventDimethylformamideHCID 6228—
ProductHCID 14074120HCID 1407412059%

Reaction Conditions

Temperature90 °C

Reaction Steps

2.21 g (6 mmol) of 1-(4-hydroxy-3,5-dimethylphenyl)piperazine dihydrobromide, 1.14 g (6.25 mmol) of 2-chloro-5-trifluoromethylpyridine and 1.245 g (9 mmol) of K2CO3 in 27 ml of absolute DMF were reacted by the same procedure as described in Example 20. The mixture was subsequently stirred for 3.5 hours at 90° C. After evaporation of the DMF, the residue was mixed with water, and the oily crystalline material produced during this was filtered off under suction, dissolved in methanol and clarified using activated charcoal. After filtration, a little water was added to the filtrate, a crystalline precipitate being produced. This was filtered off under suction (yield 1.63 g) and chromatographed as described in Example 15 on a silica gel/CH2Cl2 column (diameter 2.0 cm, height 22 cm). In this fashion, 1.24 g (=59% yield) of 1-(4-hydroxy-3,5-dimethylphenyl)-4-(5-trifluoromethylpyrid-2-yl)piperazine, melting point 143°-44° C., were obtained;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04824846
Source datasetuspto-grants-1989_04
ORD IDord-32d7a4b8906a419fb93f0d98f09d1097
Source noteuspto-grants-1989_04