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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(4-(tert-Butoxycarbonyl)piperazin-1-yl)propanoic acid | HCID 2735645 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Tert-butyl 4-(1-hydroxypropan-2-yl)piperazine-1-carboxylate | HCID 50987509 | 33.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737149B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-685cd1e0359a40c1a4d29e642a6d5327 |
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| Source note | uspto-grants-2010_06 |
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