HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657180Generated: November 2, 2026
Dimethyl Sulfoxide → HCID 53878410, compound
https://huagongshe.com/reaction/1657180
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Fluorobenzaldehyde | HCID 68023 | — |
| Reactant | 1-[2-(2-Hydroxyethoxy)ethyl]piperazine | HCID 139436 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 53878410 | HCID 53878410 | 96% |
Reaction Steps
A mixture of 54.3 grams (0.61 mol) of N-[2'-(2"-hydroxyethoxy)ethyl]piperazine, 50 grams (0.40 mol) of 4-fluorobenzaldehyde, 50 grams of anhydrous potassium carbonate, and 50 mL of DMSO was heated to 120° C. for four days under nitrogen. After cooling to room temperature, the solution was diluted with one liter of water. The aqueous solution was "processed" as follows. It was extracted with dichloromethane; the separated organic layers were combined and dried over anhydrous magnesium sulfate or sodium sulfate. The organic layer was separated, and solvent was removed on a rotary evaporator under reduced pressure (hereafter these steps will be referred to as "processed" and the product was dried under vacuum overnight to afford 75.3 grams (96%) of 4-[4'-(2"-(2'"-hydroxyethoxy)ethyl)piperazino]benzaldehyde (F).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05256784 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-2790da6d08f9406bb8ba0df8786b98b4 |
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| Source note | uspto-grants-1993_10 |
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