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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16839Generated: October 29, 2026

2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)propanoic acid → Tert-butyl 4-(1-hydroxypropan-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/16839

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)propanoic acidHCID 2735645—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(1-hydroxypropan-2-yl)piperazine-1-carboxylateHCID 5098750933.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

A 1M solution of borane tetrahydrofuran complex (12.00 mL, 12.00 mmol) in THF, was added dropwise to a stirred suspension of 2-(1-tert-butoxycarbonylpiperazin-4-yl)propionic acid (2.58 g, 10 mmol) in tetrahydrofuran (50 mL) at 0° C., over a period of 10 mins under nitrogen. The resulting solution was stirred at 60° C. for 8 h. This was quenched with acetic acid/water (10 ml, 1:2 mixture) and evaporated to dryness. The residue was dissolved in ethyl acetate (50 ml), washed with saturated sodium bicarbonate (25 ml) and water, dried over MgSO4, filtered and evaporated to dryness to give tert-butyl 4-(1-hydroxypropan-2-yl)piperazine-1-carboxylate (0.810 g, 33.2%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737149B2
Source datasetuspto-grants-2010_06
ORD IDord-685cd1e0359a40c1a4d29e642a6d5327
Source noteuspto-grants-2010_06