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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119355Generated: November 1, 2026

Hydrochloric Acid → HCID 9167299, compound

https://huagongshe.com/reaction/2119355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHexahydro-1,4-diazepineHCID 68163—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
ReactantEthanol hydrochlorideHCID 21887872—
SolventEthanolHCID 702—
ProductHCID 9167299HCID 9167299—

Reaction Steps

To a solution of homopiperazine (9.2 g, 92 mmol, 2 equiv). in EtOH (115 mL) was added 1 M HCl-EtOH (92 mL) dropwise over 1 h. The suspension was heated to 70° C. for 1 h at which point a homogeneous solution of monohydrochloride salt was obtained. α-Bromo-p-tolunitrile (9.0 g, 46 mnmol, 1 equiv) was added and the reaction mixture was heated to reflux for 5 h. After cooling, the solvent was removed by rotary evaporation and the residue was partitioned between CH2Cl2 (100 mL) and 2N aqueous KOH (100 mL). The aqueous layer was extracted with CH2Cl2 (5×50 mL) and the combined organic phase was washed with saturated aqueous NaCl (1×150 mL) and dried (MgSO4). Chromatography (SiO2, 4×20 cm, 20% CH3OH —5% Et3N—CH2Cl2) afforded the desired monoalkylated material (6.78 g, 10.1 g theoretical, 67%) as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686353B1
Source datasetuspto-grants-2004_02
ORD IDord-9cc9bbaba619437f83c52ec490707827
Source noteuspto-grants-2004_02