HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175760Generated: October 27, 2026
tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate → tert-butyl(3S)-3-(hydroxymethyl)-4-[2-hydroxy-2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate
https://huagongshe.com/reaction/2175760
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate | HCID 24820294 | — |
| Reactant | 5-(oxiran-2-yl)-2-benzofuran-1(3H)-one | HCID 59568715 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-butyl(3S)-3-(hydroxymethyl)-4-[2-hydroxy-2-(1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-carboxylate | HCID 71271745 | — |
Reaction Steps
5-(Oxiran-2-yl)-2-benzofuran-1(3H)-one (1.5 g, 8.5 mmol) and commercially available (S)-4-N-BOC-2-hydroxymethyl piperazine (2.394 g, 11.07 mmol) were combined in ethanol (10 mL) in a microwave tube. The mixture was degassed then heated for 60 min at 150° C. LC-MS showed the product peak. The reaction was worked up by adding ethyl acetate and washing once with brine. The organic layer was separated, dried, and concentrated to dryness. The crude product was purified by MPLC using an 80 g Redi-sep column and eluted with 50%-100% EtOAc/hexane yielding the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09062070B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-dbcb715b91484763a492f7004b47a873 |
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| Source note | uspto-grants-2015_06 |
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