HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014192Generated: October 30, 2026
Potassium Carbonate → HCID 59860244, compound
https://huagongshe.com/reaction/1014192
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Fluoro-2-nitroanisole | HCID 2779250 | — |
| Reactant | (3S)-Piperidin-3-ol--hydrogen chloride (1/1) | HCID 16211918 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Product | HCID 59860244 | HCID 59860244 | 78.3% |
Reaction Steps
A solution of (3S)-3-piperidinol hydrochloride (3.00 g, 21.7 mmol, Astatech Inc.), 4-fluoro-2-(methyloxy)-1-nitrobenzene (3.38 g, 19.76 mmol) and potassium carbonate (9.00 g, 65.22 mmol) in dimethylsulfoxide (75 mL) was stirred overnight. The next morning, the reaction was diluted with diethyl ether and saturated aqueous sodium chloride. The ether layer was washed with water, and the combined aqueous layers were subsequently washed twice with diethyl ether. The combined organic layers were dried over sodium sulfate, filtered, taken to a residue under reduced pressure, and purified by chromatography on SiO2 (5% MeOH/CH2CL2) to give (3S)-1-[3-(methyloxy)-4-nitrophenyl]-3-piperidinol as a pale yellow solid (3.90 g, 15.47 mmol, 78% yield). 1H NMR (400 MHz, CDCl3) δ ppm 1.59-1.71 (m, 2 H), 1.79 (s, 1 H), 1.86-1.96 (m, J=12.96, 6.41, 6.27, 3.48 Hz, 1 H), 1.96-2.04 (m, 1 H), 3.13-3.24 (m, 2 H), 3.47 (ddd, J=12.59, 6.36, 3.20 Hz, 1 H), 3.66 (dd, J=12.82, 3.48 Hz, 1 H), 3.86-3.92 (m, J=7.44, 3.94, 3.74, 3.74 Hz, 1 H), 3.93 (s, 3 H), 6.34 (d, J=2.56 Hz, 1 H), 6.43 (dd, J=9.34, 2.38 Hz, 1 H), 7.98 (d, J=9.34 Hz, 1 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07981903B2 |
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| Source dataset | uspto-grants-2011_07 |
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| ORD ID | ord-852a6063d0f744aabf70f987399fdf72 |
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| Source note | uspto-grants-2011_07 |
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