Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374738Generated: October 25, 2026

Sodium Hydroxide → 2-(4-Benzylpiperazin-2-yl)ethanol

https://huagongshe.com/reaction/1374738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfateHCID 24436—
Reactant(RS)-ethyl-(4-benzylpiperazin-2-yl)acetateHCID 21077878—
ReactantAluminium lithium hydrideHCID 21226445—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Benzylpiperazin-2-yl)ethanolHCID 2202195391.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166608B2
Source datasetuspto-grants-2007_01
ORD IDord-f4afc4719a024cb28b09b6415dcac3ff
Source noteuspto-grants-2007_01