HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066548Generated: October 31, 2026
Potassium Carbonate → HCID 66870241, compound
https://huagongshe.com/reaction/2066548
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Oxolan-3-yl methanesulfonate | HCID 15278452 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 66870241 | HCID 66870241 | — |
Reaction Steps
To tetrahydro-furan-3-ol (1.0 g, 11.4 mmol) in anhydrous dichloromethane (15 mL) with triethylamine (2.37 mL, 17.03 mmol), was added methane sulfonyl chloride (12.5 mmol) at 0° C. The reaction mixture was stirred at RT for 3.5 hours, diluted with dichloromethane (50 mL) and washed with water. The organic phase was dried (MgSO4) and evaporated in-vacuo to give methanesulfonic acid tetrahydro-furan-3-yl ester as light orange oil (1.68 g, 89%). A mixture of piperazine-1-carboxylic acid tert-butyl ester (1.0 g, 5.38 mmol), methanesulfonic acid tetrahydrofuran-3-yl ester (1.07 g, 6.45 mmol) and K2CO3 (2.96 g, 21.5 mmol) was stirred in anhydrous acetonitrile (50 mL) under reflux conditions for 12 hours. The reaction mixture was cooled and poured onto water and extracted with dichloromethane to give after silica chromatography, 4-(tetrahydro-furan-3-yl)-piperazine-1-carboxylic acid tert-butyl ester, as a colourless oil (0.57 g, 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08293735B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-05ec5fc1519c4a6b97c5980ef997c928 |
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| Source note | uspto-grants-2012_10 |
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