HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584217Generated: November 1, 2026
1,2-Dimethoxyethane → HCID 22342949, compound
https://huagongshe.com/reaction/584217
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 22342720 | HCID 22342720 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22342949 | HCID 22342949 | 86.1% |
Reaction Steps
A suspension of 3-(2,3-dimethoxybenzyl)-2,5-piperazinedione (1.26 g) in a mixed solvent of tetrahydrofuran (50 ml) and 1,2-dimethoxyethane (50 ml) was heated at 60° C. with stirring and lithium aluminum hydride (0.905 g) was added thereto portionwise carefully. After the reaction mixture was heated at 70° C. with stirring for 3 hours, lithium aluminum hydride (0.20 g) and tetrahydrofuran (30 ml) were added thereto again and the suspension was stirred at the same temperature for 12 hours. After being cooled with ice-water, the mixture was quenched by sequential addition of water (1.3 ml), 15% aqueous sodium hydroxide (1.3 ml), water (3.8 ml) and the whole was stirred at room temperature for 2 hours. The resulting insoluble materials were removed by filtration and the filtrate was dried over sodium sulfate, and evaporated under reduced pressure to give light yellowish oil of 2-(2,3-dimethoxybenzyl)piperazine (0.97 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06924278B2 |
|---|
| Source dataset | uspto-grants-2005_08 |
|---|
| ORD ID | ord-6c1b8e68bcdd4fe09286bf9cb7d4f886 |
|---|
| Source note | uspto-grants-2005_08 |
|---|