HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13536Generated: October 25, 2026
Tetrahydrofuran → 1-(4-Formylbenzoyl)-4-isopropylpiperazine
https://huagongshe.com/reaction/13536
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Isopropylpiperazine | HCID 78013 | — |
| Reactant | 4-Formylbenzoyl chloride | HCID 12424620 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-Formylbenzoyl)-4-isopropylpiperazine | HCID 57478581 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728129B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-aec267aab7a3492ea2e6faaccc86e556 |
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| Source note | uspto-grants-2010_06 |
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