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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838239Generated: October 30, 2026

Tetrahydrofuran → (2R,5S)-1-benzyl-2,5-dimethylpiperazine

https://huagongshe.com/reaction/1838239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant(3S,6R)-1-benzyl-3,6-dimethylpiperazine-2,5-dioneHCID 11673088—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
Product(2R,5S)-1-benzyl-2,5-dimethylpiperazineHCID 1063202885.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

In an atmosphere of argon, 0.57 g of lithium aluminum hydride was added at 0° C. to 30 ml of THF solution containing 1.0 g of (3S,6R)-1-benzyl-3,6-dimethylpiperazine-2,5-dione, and the mixture was stirred overnight with heating under reflux. The reaction mixture was cooled to 0° C., 1.0 ml of water was added dropwise thereto and 1.0 ml of 10% aqueous sodium hydroxide was added dropwise thereto, and then the mixture was further mixed with 1.0 ml of water and stirred for 30 minutes. The precipitate was separated by filtration and washed with ethyl acetate, and the filtrate was washed with 10% aqueous potassium carbonate and saturated brine, dried over anhydrous magnesium sulfate, filtered and then concentrated. The residue was subjected to a silica gel column chromatography and eluted with chloroform-methanol-28% aqueous ammonia (25:1:0.1, v/v/v) to obtain 0.75 g of the title compound as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673799B1
Source datasetuspto-grants-2004_01
ORD IDord-82e08a76750a4893b775c813a58a4ed4
Source noteuspto-grants-2004_01