HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555234Generated: October 25, 2026
1-Hydroxypiperidine → 2-Cyclohexylpiperidin-1-ol
https://huagongshe.com/reaction/555234
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Hydroxypiperidine | HCID 20935 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178478990 | HCID 178478990 | — |
| Catalyst | Manganese dioxide | HCID 14801 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Cyclohexylpiperidin-1-ol | HCID 17988795 | 27% |
Reaction Steps
Activated MnO2 (1.29 g, 14.8 mmol) was added to a solution of N-hydroxypiperidine (0.50 g, 4.95 mmol) in dichloromethane (25 mL) at 0° C. and the mixture was stirred for 1 h. The reaction mixture was filtered through a pad of Celite™ and Na2SO4. The filtrate was added dropwise to a solution of cyclohexylmagnesium chloride (2.0 M in diethyl ether, 4.95 mL, 9.90 mmol) at −10° C. The reaction mixture was stirred at 0° C. for 0.5 h and then saturated aqueous ammonium chloride solution (25 mL) and dichloromethane (25 mL) were added. The aqueous phase was separated and extracted with dichloromethane (2×30 mL). The combined organic layers were dried (Na2SO4) and concentrated under reduced pressure. The crude product was subjected to flash chromatography on SiO2 eluting with 40% diethyl ether in hexanes to give the title compound (0.241 g, 27%) as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08053432B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-4dd1c8ea680742bd8d0428c702d2aa3f |
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| Source note | uspto-grants-2011_11 |
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