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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703401Generated: October 25, 2026

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

https://huagongshe.com/reaction/1703401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPiperazineHCID 4837—
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
Reactant2,3-Dihydro-1,4-benzodioxin-2-carbonyl chlorideHCID 2735447—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product1-(1,4-Benzodioxan-2-ylcarbonyl)piperazine hydrochlorideHCID 282243412.3%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04351940
Source datasetuspto-grants-1982_09
ORD IDord-d25f81b2204c4f55b5ba6054dfba9a05
Source noteuspto-grants-1982_09