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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (3S,6R)-1-benzyl-3,6-dimethylpiperazine-2,5-dione | HCID 11673088 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Product | (2R,5S)-1-benzyl-2,5-dimethylpiperazine | HCID 10632028 | 85.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06673799B1 |
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| Source dataset | uspto-grants-2004_01 |
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| ORD ID | ord-82e08a76750a4893b775c813a58a4ed4 |
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| Source note | uspto-grants-2004_01 |
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