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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1293525Generated: October 30, 2026

Acetic Acid → tert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylate

https://huagongshe.com/reaction/1293525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPiperidin-4-olHCID 79341—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 4-hydroxy-[1,4'-bipiperidine]-1'-carboxylateHCID 9835508—

Reaction Steps

To 1-tert-butoxycarbonyl-4-piperidone (200 g, 1.01 mol) in tetrahydrofuran (THF) (1500 ml) was added 4-hydroxypiperidine (78.1 g, 0.77 mol). The resultant slurry was stirred for 30 minutes before cooling the reaction mixture with ice/water, acetic acid (47 ml) is then added (exotherm) which caused precipitation. The slurry was allowed to warm to room temperature before the addition of sodium triacetoxyborohydride (236 g, 1.12 mol) which was washed in with THF (500 ml). The resultant slurry was stirred overnight at room temperature. To the reaction mixture was added water (2000 ml) to give a solution. The solution was then extracted with diethyl ether (3×1800 ml). The aqueous phase was basified with 10% aq NaOH (950 ml) and extracted with dichloromethane (DCM) (3×1500 ml). The combined DCM layers are dried (MgSO4), filtered and the solvent removed to give the sub-titled compound as a yellow viscous oil, (177 g, 81%; MS: (M+H) 285).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07238811B2
Source datasetuspto-grants-2007_07
ORD IDord-1db916f3b09942f18dee1bb224847a92
Source noteuspto-grants-2007_07