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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 54202Generated: October 29, 2026

1-(2-Methoxyphenyl)-4-(1-(4-phenylphenyl)cyclohex-1-en-4-yl)piperazine → HCID 178489564, compound

https://huagongshe.com/reaction/54202

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)-4-(1-(4-phenylphenyl)cyclohex-1-en-4-yl)piperazineHCID 19958551—
CatalystPalladiumHCID 23938—
SolventAcetic AcidHCID 176—
ProductHCID 178489564HCID 178489564—

Reaction Steps

1-(2-Methoxyphenyl)-4-(1-(4-phenylphenyl)cyclohex-1-en-4-yl)piperazine (2.7 g, 5.4 mmol) was hydrogenated at 50 psi (about 3.5×105N.m-2) above atmospheric pressure at 45° C. in acetic acid (50 ml), using 10% Pd/C (2.4 g) as a catalyst for three days. The volatiles were evaporated in vacuo and the residue was partitioned between dichloromethane (150 ml) and sat. NaHCO3 (200 ml). The organic layer was separated and washed with brine and evaporated in vacuo. The residues were recrystallised from dichloromethane and again from methanol. The white solid was dissolved in ether and acidified to pH 1 with ethereal HCl. The volatiles were removed in vacuo to give the title compound as the one and a half hydrochloride; three quarters hydrate (0.281 g), m.p. 220°-225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05622951
Source datasetuspto-grants-1997_04
ORD IDord-d55d7cc28e1a48f58fe03a4724d0e591
Source noteuspto-grants-1997_04