HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 750465Generated: October 25, 2026
Sodium Hydroxide → 2-(4-Benzylpiperazin-2-yl)ethanol
https://huagongshe.com/reaction/750465
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | (RS)-ethyl-(4-benzylpiperazin-2-yl)acetate | HCID 21077878 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(4-Benzylpiperazin-2-yl)ethanol | HCID 22021953 | 91.3% |
Reaction Steps
A 1M solution of lithium aluminium hydride in tetrahydrofuran (32.8 ml) was added dropwise to a stirred solution of (RS)-ethyl-(4-benzylpiperazin-2-yl)acetate (D3) (4.3 g, 16.41 mmol) in anhydrous tetrahydrofuran (100 ml) under argon, maintaining the temperature below 10° C. The resultant was stirred for a further 0.25 h, warmed to room temperature and stirred for 2.5 h. Water (8.2 ml), 2N sodium hydroxide (10.2 ml), and water (8.2 ml) were added dropwise sequentially with ice cooling. After 0.2 h sodium sulfate was added, the mixture stirred for 0.2 h then filtered through a short pad of celite. The filtrate was evaporated in vacuo to give the title compound as a pale orange oil (3.3 g, 91%). Mass spectrum (AP+): Found 221 (MH+). C13H20N2O requires 220.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07405217B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-fd06224e8f464a368b33f53fa827df48 |
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| Source note | uspto-grants-2008_07 |
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