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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893398Generated: October 29, 2026

Iodine → HCID 20077842, compound

https://huagongshe.com/reaction/893398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantBromobenzeneHCID 7961—
ReactantMagnesiumHCID 5462224—
ReactantHCID 22314793HCID 22314793—
Catalyst1,2-DibromoethaneHCID 7839—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20077842HCID 20077842—

Reaction Steps

To bromobenzene (0.6 g) and magnesium turnings (0.2 g) in 30 ml dry tetrahydrofuran under nitrogen was added a small crystal of iodine and 10 drops of 1,2-dibromoethane. After small bubbles began to form, the reaction was stirred and heated to reflux for 4 hours. After cooling to room temperature, 1-benzyl-4-(1-cyanocyclohexyl)piperazine (1 g) was added. After 23 hours, the reaction was filtered, 20 ml saturated aqueous ammonium chloride was added and the mixture was extracted with diethyl ether. The ether was dried and removed in vacuo. The residue was chromatographed on silica gel eluted with chloroform to yield pure 1-benzyl-4-(1-phenylcyclohexyl)piperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05124457
Source datasetuspto-grants-1992_06
ORD IDord-7cacdca12b5d43c194d041a46c6675f4
Source noteuspto-grants-1992_06