HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004569Generated: October 25, 2026
Triethylamine → (+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazine
https://huagongshe.com/reaction/1004569
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,5-Dimethylbenzoic acid | HCID 10356 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 2-(3,4-Dichlorophenyl)piperazine | HCID 4231356 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (+)-(3,5-Dimethylbenzoyl)-3-(3,4-dichlorophenyl)piperazine | HCID 10292159 | 57.8% |
Reaction Steps
To a cooled solution of CH2Cl2 (600 mL) containing 2-(3,4-dichlorophenyl)piperazine (6.934 g, 30 mmol), 3,5-dimethylbenzoic acid (4.55 g, 30 mmol), and N-hydroxybenzotriazole monohydrate (4.05 g, 30 mmol) at -20° C. were added Et3N (4.2 mL, 30 mmol) and N,N-dimethylaminopropylethylcarbodimide (DEC) (5.86 g, 30 mmol) under nitrogen. The reaction was kept at -20° C. for an hour and gradually warmed to RT overnight. After stirring 22 hours, the reaction was complete and CH2Cl2 (200 mL) was added. The organic solution was washed with brine (150 mL, 3×), dried over MgSO4, filtered and concentrated under vacuum to give 8.2 g of crude product. The product was crystallized from CH2Cl2 /Hexane to give a light yellow solid (6.3 g, 17.34 mmol, 57.8%). Mm.p.139-141° C.; FAB MS [M+1]+35Cl 363.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06051575 |
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| Source dataset | uspto-grants-2000_04 |
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| ORD ID | ord-f83c28f0b5ee407aa13c4f0398fad8a3 |
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| Source note | uspto-grants-2000_04 |
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