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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911411Generated: November 3, 2026

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

https://huagongshe.com/reaction/1911411

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 numberUS08604022B2
Source datasetuspto-grants-2013_12
ORD IDord-683eee72b332451f83077b7e65bc4a2b
Source noteuspto-grants-2013_12