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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555234Generated: October 25, 2026

1-Hydroxypiperidine → 2-Cyclohexylpiperidin-1-ol

https://huagongshe.com/reaction/555234

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxypiperidineHCID 20935—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 178478990HCID 178478990—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
Product2-Cyclohexylpiperidin-1-olHCID 1798879527%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053432B2
Source datasetuspto-grants-2011_11
ORD IDord-4dd1c8ea680742bd8d0428c702d2aa3f
Source noteuspto-grants-2011_11