HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1752237Generated: October 28, 2026
HCID 71212260, compound → (4-Methoxy-3-methylphenyl)-4-piperidinylmethanone
https://huagongshe.com/reaction/1752237
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 71212260 | HCID 71212260 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | (4-Methoxy-3-methylphenyl)-4-piperidinylmethanone | HCID 20613914 | — |
Reaction Steps
A suspension of 1-(4-(4-methoxy-3-methylbenzoyl)piperidin-1-yl)ethanone (5.45 g, 19.8 mmol) in 6 N HCl (40 mL) was heated to reflux for 12 h then concentrated in vacuo to a light purple solid. The material was taken up in ˜100 mL MeOH with heating and sonication, concentrated in vacuo to ˜25 mL, added diethyl ether (˜200 mL) to form white precipitate and a purple aqueous layer. The aqueous layer was removed via a pipet and concentrated in vacuo. The suspension was decanted through filter to recover a white solid (1.30 g). The aqueous material was concentrated in vacuo to form a purplish oil which was taken up in diethyl ether and the resulting suspension was filtered (0.82 g). The filtrate was concentrated in vacuo to a purple oil. The solid material was confirmed to be the title compound. Calculated molecular formula=C14H19NO2=233.31. found MS (ESI) m/e 233.9 (M+H+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09163003B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-ada828c924f34f35ba097c66d5e0ccc1 |
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| Source note | uspto-grants-2015_10 |
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