Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374989Generated: October 31, 2026

HCID 53871969, compound → HCID 53740990, compound

https://huagongshe.com/reaction/1374989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 53871969HCID 53871969—
CatalystHCID 178502593HCID 178502593—
SolventMethanolHCID 887—
ProductHCID 53740990HCID 5374099098.4%

Reaction Steps

A mixture of (2R)-4-benzyl-1-[3,5-bis(trifluoromethyl)-benzoyl]-2-[3-[(2-methoxyethoxy)methoxy]-4-methylbenzyl]-piperazine (0.38 g) in methanol (6 ml) was hydrogenated over 20% palladium hydroxide-carbon (0.06 g) at room temperature under atmospheric pressure for 8 hours. After removal of the catalyst by filtration through Celite®, the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using mixed solvents of dichloromethane and methanol (30:1). The fractions containing the objective compound were collected and evaporated under reduced pressure to give (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-[3-[(2-methoxyethoxy)methoxy]-4-methylbenzyl]piperazine (0.32 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166598B2
Source datasetuspto-grants-2007_01
ORD IDord-89e7a7b299ff45fe8d6f2fb92951f47e
Source noteuspto-grants-2007_01