HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175770Generated: October 25, 2026
tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate → (S)-tert-butyl 4-(2-hydroxy-2-(4-methyl-1-oxo-1,3-dihydroisobenzofuran-5-yl)ethyl)-3-(hydroxymethyl)piperazine-1-carboxylate
https://huagongshe.com/reaction/2175770
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-butyl (3S)-3-(hydroxymethyl)piperazine-1-carboxylate | HCID 24820294 | — |
| Reactant | 4-Methyl-5-(oxiran-2-yl)-2-benzofuran-1(3H)-one | HCID 55270555 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (S)-tert-butyl 4-(2-hydroxy-2-(4-methyl-1-oxo-1,3-dihydroisobenzofuran-5-yl)ethyl)-3-(hydroxymethyl)piperazine-1-carboxylate | HCID 71270662 | — |
Reaction Steps
4-Methyl-5-oxiran-2-yl-2-benzofuran-1(3H)-one (3.00 g, 15.8 mmol) and (S)-4-N-BOC-2-hydroxymethylpiperazine (5.12 g. 23.7 mmol) were suspended in ethanol (10 mL) in a 20 mL microwave tube. The reaction mixture was degassed and heated in a microwave apparatus for 30 min at 150° C. The reaction mixture was evaporated to dryness, then chromatographed through a 330 g Redi-sep column and eluted with a solvent system of 1:1 EtOAc/hexane to 100% EtOAc to yield the title compound. LC-MS: M+1=407.
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-89d13e1de70540799cf0a1b200d24ea0 |
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| Source note | uspto-grants-2015_06 |
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