HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225220Generated: October 30, 2026
Piperidine → 1-Methyl-4-(3-methoxyphenyl)-1,2,3,6-tetrahydropyridine
https://huagongshe.com/reaction/225220
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 4-(3-Hydroxyphenyl)-1-methyl-4-piperidinol | HCID 20534440 | — |
| Solvent | Methanesulfonic Acid | HCID 6395 | — |
| Product | 1-Methyl-4-(3-methoxyphenyl)-1,2,3,6-tetrahydropyridine | HCID 155778 | — |
Reaction Steps
To a stirred solution of 200 ml. of 50 g. of phosphorous pentoxide in methanesulfonic acid was added portionwise over four minutes 59 g. of 1-methyl-4-hydroxy-4-(3-hydroxyphenyl)piperidine. The reaction was exothermic, the temperature rising to 70° C. After complete addition of the piperidine derivative, the reaction mixture was poured onto 200 g. of ice, and the resulting aqueous mixture made alkaline by the addition of ammonium hydroxide. The alkaline mixture was extracted several times with diethyl ether, and the ethereal extracts were combined, washed with water, dried, and the solvent removed by evaporation under reduced pressure to provide 44.7 g. of an oil. The oil was distilled to provide 1-methyl-4-(3-methoxyphenyl)-1,2,5,6-tetrahydropyridine; B.P.=123°-138° C. at 0.1 torr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04236009 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-d1062ece720f40ceab4c35e4c4b504ce |
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| Source note | uspto-grants-1980_11 |
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