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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595001Generated: November 1, 2026

Lithium borohydride → Tert-butyl 4-[3-(hydroxymethyl)phenyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/595001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium borohydrideHCID 4148881—
Reactant1-Boc-4-(3-(ethoxycarbonyl)phenyl)piperazineHCID 16217941—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-[3-(hydroxymethyl)phenyl]piperazine-1-carboxylateHCID 2994934290%

Reaction Steps

tert-Butyl-4-(3-(ethoxycarbonyl)phenyl)piperazine-1-carboxylate (0.20 g, 0.60 mmol) was dissolved in THF (1 mL) and lithium borohydride (0.10 g, 7.5 eq) was added in three portions. The reaction mixture stirred at rt for 48 h then quenched with saturated ammonium chloride under ice-cooling. The aqueous phase was extracted with DCM and the combined organic phases dried over sodium sulfate and evaporated to afford tert-butyl 4-(3-(hydroxymethyl)phenyl)piperazine-1-carboxylate (0.16 mg, 0.54 mmol, 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242987B2
Source datasetuspto-grants-2016_01
ORD IDord-93e4fd56107549b5b07875aba17556c9
Source noteuspto-grants-2016_01