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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23208Erstellt: 24. Oktober 2026

Hydrochloric Acid → Methyl 4-Boc-piperazine-2-acetate

https://huagongshe.com/de/reaction/23208

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPotassium CarbonateHCID 11430—
Edukt2-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 93865—
EduktMethyl 2-(1,4-dibenzylpiperazin-2-yl)acetateHCID 22710010—
KatalysatorPalladiumHCID 23938—
LösungsmittelMethanolHCID 887—
ProduktMethyl 4-Boc-piperazine-2-acetateHCID 275681676,4%

Reaktionsschritte

The 13.7 g (40 mmol) of methyl 1,4-dibenzylpiperazine-2-acetate, 150 mL of MeOH, 50 mL of 1 N HCl (aqueous) and 3 g of 10% Pd/C were combined and hydrogenated with H2 (50 psi) for 24 hours. The reaction was filtered, the filtrate was concentrated in vacuo to remove most of the MeOH, and the residue was made basic with K2CO3 to pH=9-10, and 9.8 g (40 mmol) of BOC-ON was added slowly at 0° C. The reaction was stirred at 0° for 1 hour, allowed to warm up to room temperature, stirred for 2 hours, and extracted with ethyl acetate (2×200 mL). The combined extracts were treated with 50 mL of 10% HCl (aqueous). The aqueous layer was washed with ethyl acetate, basified with K2CO3 and extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo to give 7.89 g of methyl 4-Boc-piperazine-2-acetate; 1H NMR (CDCl3) δ 1.4 (s,9), 2.31 (dd,1), 2.37 (dd, 1), 2.55 (b, 1), 2.69-3.02 (m,4), 3.75 (s,3), 3.88 (b, 2).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06849739B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-a859f4b242f8477099a02a6606c472aa
Quellennotizuspto-grants-2005_02