HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262311Generated: November 3, 2026
Potassium Carbonate → 1-(3-Methoxy-4-nitro-benzyl)-piperidin-4-ol
https://huagongshe.com/reaction/1262311
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | 3-Methoxy-4-nitrobenzyl bromide | HCID 12621604 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(3-Methoxy-4-nitro-benzyl)-piperidin-4-ol | HCID 66711686 | — |
Reaction Steps
Into a 8-dram vial, 4-Bromomethyl-2-methoxy-1-nitro-benzene (2.44 g, 9.93 mmol), Piperidin-4-ol (2.01 g, 19.9 mmol), Potassium carbonate (5.49 g, 39.7 mmol), and N,N-Dimethylformamide (25 ml) were added. The reaction mixture was heated at 80° C. overnight. The reaction was partitioned with water and EtOAc. The organic was separated, washed with Brine and dried over Na2SO4. The solid was filtered and washed with DCM. The solvent was removed under vacuum. The reaction mixture was purified via ISCO column chromatography with hexane and EtOAc as eluant (0 to 100% EtOAc). The collected fractions afforded 1-(3-Methoxy-4-nitro-benzyl)-piperidin-4-ol as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08471005B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-ec91ab89b2894839a1ed837692d51076 |
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| Source note | uspto-grants-2013_06 |
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