HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375533Generated: October 25, 2026
4-Hydroxybenzaldehyde → Benzaldehyde, 4-(3-(4-phenyl-1-piperazinyl)propoxy)-
https://huagongshe.com/reaction/375533
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Piperazine, 1-(3-chloropropyl)-4-phenyl- | HCID 139197 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Benzaldehyde, 4-(3-(4-phenyl-1-piperazinyl)propoxy)- | HCID 55234 | 69.6% |
Reaction Steps
Sodium hydride (3.59 g of 60% in oil) is added to 4-hydroxybenzaldehyde (9.95 g) in dimethylformamide (250 mL) and the mixture stirred at 60° C. for 30 minutes. 1-(3-Chloropropyl)-4-phenylpiperazine (Step A) (19.5 g) is added and the mixture stirred for 14 hours at 60° C. The solvent is evaporated and the residue treated with water (300 mL) and extracted with dichloromethane (3×150 mL). The extracts are dried over magnesium sulfate, filtered and evaporated to leave a beige solid. This solid is recrystallized from ethyl acetate/diethyl ether to give 18.4 g of the title compound as a light beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05486517 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-0498d120f60344b48fdaa4502b8c9272 |
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| Source note | uspto-grants-1996_01 |
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