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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919155Generated: November 1, 2026

Aluminium lithium hydride → (4-Benzyl-1-methylpiperazin-2-yl)methanol

https://huagongshe.com/reaction/1919155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 49766299HCID 49766299—
SolventTetrahydrofuranHCID 8028—
Product(4-Benzyl-1-methylpiperazin-2-yl)methanolHCID 1977724791.1%

Reaction Steps

To a solution of 336a (1 g, 2.99 mmol) in 100 mL of anhydrous tetrahydrofuran was slowly added lithium aluminum hydride (342 mg, 8.98 mmol) at 0° C. and the mixture was stirred for 30 min. Then, it was refluxed for 3 h and the reaction mixture was poured onto ice portionwise. The resulting mixture was filtered and the filtrate was evaporated in vacuo. After addition of 100 mL brine to the residue, it was extracted with methylene chloride (100 mL×3). The combined organic layer was dried over Na2SO4, filtered, and concentrated to afford 336b as yellow oil (0.60 g, 91%). MS: [M+H]+ 221.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618107B2
Source datasetuspto-grants-2013_12
ORD IDord-f08b3461871841f3b85b01effb84d1a6
Source noteuspto-grants-2013_12