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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8746Generated: October 26, 2026

Methyl 4-(4-oxobut-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate → 4-(1-(tert-Butoxycarbonyl)-4-(methoxycarbonyl)piperidin-4-yl)butanoic acid

https://huagongshe.com/reaction/8746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(4-oxobut-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylateHCID 86597419—
ReactantJones' reagentHCID 131709961—
SolventAcetoneHCID 180—
Product4-(1-(tert-Butoxycarbonyl)-4-(methoxycarbonyl)piperidin-4-yl)butanoic acidHCID 21983987—

Reaction Steps

To a solution of methyl 4-(4-oxobut-1-yl)-1-(tert-butoxycarbonyl)piperidine-4-carboxylate (23.0 g, 0.0734 mol) from Step C in acetone (775 mL) at room temperature was added Jones reagent (28.2 mL, 2.6M) via syringe. After 5 min, the reaction mixture was concentrated. The residue was taken up in water and diethyl ether and extracted three times with diethyl ether. The organic layers were combined, washed with brine, dried over sodium sulfate, filtered, and concentrated to give the title compound (23.4 g) which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07091211B2
Source datasetuspto-grants-2006_08
ORD IDord-190dcd50c65c412eb9c6458f3623a7b2
Source noteuspto-grants-2006_08