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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1092064Erstellt: 26. Oktober 2026

Trimethylsilyldiazomethane → Methyl 4-((4-methylpiperazin-1-yl)methyl)benzoate

https://huagongshe.com/reaction/1092064

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilyldiazomethaneHCID 167693—
Edukt4-(4-Methyl-1-piperazinylmethyl)benzoic acidHCID 4769782—
LösungsmittelMethanolHCID 887—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl 4-((4-methylpiperazin-1-yl)methyl)benzoateHCID 78222244,2%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08129391B2
Quelldatensatzuspto-grants-2012_03
ORD IDord-4d95eaf64740474096573688ff61119a
Quellennotizuspto-grants-2012_03