HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594370Generated: October 31, 2026
Methanesulfonic Acid → 6-(4-Chloro-2,6-dimethoxyphenyl)piperidin-2-one
https://huagongshe.com/reaction/594370
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | 1-Chloro-3,5-dimethoxybenzene | HCID 81502 | — |
| Reactant | (S)-6-Oxo-2-piperidinecarboxylic acid | HCID 11126383 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(4-Chloro-2,6-dimethoxyphenyl)piperidin-2-one | HCID 69085048 | — |
Reaction Steps
A mixture of commercially available 1-chloro-3,5-dimethoxybenzene (1.243 g; 6.98 mmol), P2O5(991 mg; 6.98 mmol), and methanesulfonic acid (5.659 g; 58.89 mmol) was treated with commercially available (S)-6-oxopiperidine-2-carboxylic acid (1.000 g; 6.98 mmol), and the resulting mixture was heated to 100° C. for 30 min. After cooling to rt, water was added, and the resulting solution was extracted with DCM. The mixed organic layers were dried over anh. MgSO4, filtered, and concentrated to dryness under reduced pressure. Purification by preparative HPLC afforded 6-(4-chloro-2,6-dimethoxyphenyl)piperidin-2-one as a colorless solid. LC-MS (conditions E): tR=0.61 min.; [M+H]+: 270.26 g/mol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242970B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-11dd0bceafb14a0ba3cb616aabca4bb2 |
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| Source note | uspto-grants-2016_01 |
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