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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13536Generated: October 25, 2026

Tetrahydrofuran → 1-(4-Formylbenzoyl)-4-isopropylpiperazine

https://huagongshe.com/reaction/13536

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant1-IsopropylpiperazineHCID 78013—
Reactant4-Formylbenzoyl chlorideHCID 12424620—
SolventWaterHCID 962—
Product1-(4-Formylbenzoyl)-4-isopropylpiperazineHCID 57478581—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

4-Isopropyl-piperazine (79.53 g, 0.620 mol), THF (444 g, 5.04 mol), water (36 g, 2 mol) and a 50% solution of sodium hydroxide (130.6 g, 1.63 mol) were charged to a reaction vessel and cooled to 0-5° C. 4-Formyl-benzoyl chloride in THF (110.08 g, 0.630 mol) was added to the 4-isopropyl-piperazine reaction mixture while maintaining the temperature below about 10° C. The resulting white suspension was stirred at room temperature until the reaction was deemed complete. Water was added to the reaction slurry and the resulting hazy solution was filtered over Celite to remove insolubles. The filtered reaction solution was settled and the water layer was removed. The product/THF layer was dried sequentially with magnesium sulfate and molecular sieves. The product solution (KF≦0.5%) was stored at 5° C. for use without further manipulations.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728129B2
Source datasetuspto-grants-2010_06
ORD IDord-aec267aab7a3492ea2e6faaccc86e556
Source noteuspto-grants-2010_06