HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16794Erstellt: 24. Oktober 2026
Trimethylsilyldiazomethane → Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoate
https://huagongshe.com/de/reaction/16794
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Trimethylsilyldiazomethane | HCID 167693 | — |
| Edukt | 4-(4-Methyl-1-piperazinylmethyl)benzoic acid | HCID 4769782 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoate | HCID 782222 | 44,2% |
Reaktionsschritte
A solution of (trimethylsilyl)diazomethane ((0.611 mL, 3.84 mmol) 2.0M in diethyl ether) was added dropwise to a stirred suspension of 4-((4-methylpiperazin-1-yl)methyl)benzoic acid (0.75 g, 3.20 mmol) in toluene (21 mL) and methanol (7 mL) over a period of 10 mins under nitrogen. The resulting suspension was stirred at room temperature for 3 h. A further aliquot of (trimethylsilyl)diazomethane (1.222 mL, 7.68 mmol) was added dropwise and the solution was stirred at room temperature for a further 18 h. The reaction mixture was evaporated to dryness to afford the crude product (0.723 g) as a white solid. This was taken up in DCM and the insolubles were filtered off. The filtrate was evaporated to dryness to afford the crude product. This was taken up in DCM again and more insolubles were filtered off to afford methyl 4-((4-methylpiperazin-1-yl)methyl)benzoate (0.351 g, 44.2%), which was used without purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737149B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-37f83163a3964c7e86f2f9cd86e5db68 |
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| Quellennotiz | uspto-grants-2010_06 |
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