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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222327Generated: October 31, 2026

Tert-butyl 4-hydroxypiperidine-1-carboxylate → Ammonia

https://huagongshe.com/reaction/222327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 643502—
Reactant4-Chloro-2,3-dimethylpyridineHCID 22660262—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDimethyl SulfoxideHCID 679—
ProductAmmoniaHCID 222—
ProductHCID 57753825HCID 57753825—

Reaction Steps

Potassium tert-butoxide (4.70 g, 42 mmol) was added to a solution of 1-Boc-4-hydroxypiperidine (4.05 g, 20.1 mmol) in dimethylsulfoxide (20 mL) and the mixture was stirred at room temperature for 1 hour. 4-Chloro-2,3-dimethylpyridine (3.58 g, 20.1 mmol) was then added and the reaction mixture was stirred at 50° C. for 18 hours. The mixture was partitioned between ethyl acetate and water, and the organic layer was separated and washed with sodium hydrogen carbonate solution and brine. The organic solution was then dried over magnesium sulfate concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 94:6:0.6, to afford the title compound as an oil in 39% yield, 2.4 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207198B2
Source datasetuspto-grants-2012_06
ORD IDord-42d67a2c98154db5a959f15a5c04ea5b
Source noteuspto-grants-2012_06