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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1494398Generated: November 2, 2026

Piperazine → HCID 67829624, compound

https://huagongshe.com/reaction/1494398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant6,7-Dichloro-2-tetraloneHCID 4452853—
SolventTolueneHCID 1140—
ProductHCID 67829624HCID 6782962446.1%

Reaction Steps

A mixture consisting of 6,7-dichloro-2-tetralone (4.30 g), piperazine (3.44 g), and 4A molecular sieves (4 g) 100 ml of toluene was stirred overnight under nitrogen and warmed briefly. The sieves were filtered off, and the filtrate was freed of solvent on an evaporator. Seventy-five ml of THF and 6 ml of methanol were added to the residue. The solution was cooled in an ice bath under nitrogen, and 1.24 g of sodium cyanoborohydride was added. Small amounts of gaseous HCl were added periodically until the solution remained acidic. The solution was stirred overnight at ambient temperature, the solvents were evaporated, and the residue was dissolved in dilute HCl. The acidic solution was extracted with three portions of ether and then made basic with sodium hydroxide. The oil which separated was extracted with ether, and the ether solution was dried (Na2SO4). The after evaporation of the ether was dissolved in ethanol, and excess anhydrous HCl was added. The crystalline solid isolated from the ethanol melted at about 272°-275° C. After recrystallization from ethanol there was obtained 1.1 g of the title compound. m.p. 278°-282° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05026707
Source datasetuspto-grants-1991_06
ORD IDord-4774b420b9c64f2dbc934c32f3c8478a
Source noteuspto-grants-1991_06