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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 354839Erstellt: 23. Oktober 2026

Hydrochloric Acid → 1-(1,4-Benzodioxan-2-ylcarbonyl)piperazine hydrochloride

https://huagongshe.com/de/reaction/354839

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktPiperazineHCID 4837—
EduktSodium HydroxideHCID 14798—
EduktSodium AcetateHCID 517045—
Edukt2,3-Dihydro-1,4-benzodioxin-2-carbonyl chlorideHCID 2735447—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
Produkt1-(1,4-Benzodioxan-2-ylcarbonyl)piperazine hydrochlorideHCID 282243412,3%

Reaktionsschritte

A suspension of piperazine (11.88 g.) and sodium acetate (20.30 g.) in a mixture of water (70 ml.) and acetone (95 ml.) was stirred at 10°-15° C., then concentrated hydrochloric acid was added (about 35 ml.) until the pH of the solution reached 1.5. 1,4-Benzodioxan-2-carbonyl chloride (31.0 g.) and sodium hydroxide (5 N, about 45 ml.) were then added portionwise while maintaining the temperature at 10°-15° C., the sodium hydroxide maintaining the pH at 1.7-2.2. After the addition was complete, the pH was adjusted to 2.0 by the addition of sodium hydroxide, the suspension was stirred for a further 30 minutes. Water was then added until a homogeneous solution resulted, the acetone removed in vacuo, and the aqueous phase was basified to pH 8-9 with sodium hydroxide (5 N), re-extracted with chloroform (3×200 ml.) and the extracts washed with water, dried (MgSO4) and evaporated in vacuo. The oily residue was dissolved in ethyl acetate, treated with ethereal hydrogen chloride, evaporated in vacuo and the solid residue triturated with ether, followed by recrystallization from methanol to give N-(1,4-benzodioxan-2-carbonyl)-piperazine hydrochloride (4.85 g.), M.P. 265°-267° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04377581
Quelldatensatzuspto-grants-1983_03
ORD IDord-ad716962594649ddb4f9fab4437c3eb8
Quellennotizuspto-grants-1983_03