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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81110Generated: October 31, 2026

1,8-Diazabicyclo(5.4.0)undec-7-ene → tert-Butyl 3,6-dihydropyridine-1(2H)-carboxylate

https://huagongshe.com/reaction/81110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant1-(tert-Butoxycarbonyl)-4-(methanesulfonyloxy)piperidineHCID 4184869—
SolventTetrahydrofuranHCID 8028—
Producttert-Butyl 3,6-dihydropyridine-1(2H)-carboxylateHCID 13094787—

Reaction Steps

A solution of tert-butyl 4-[(methylsulfonyl)oxy]piperidine-1-carboxylate (312 g, 1.12 mol) and DBU (400 g, 2.24 mol) in THF (4.5 L) was heated to reflux overnight. The mixture was poured into ice-water (2 L) and then extracted with EtOAc (2 L). The combined organic phase was washed with 1 M HCl solution (4 L×2), aq. NaHCO3 (4 L), and dried over anhydrous sodium sulfate. The residue was concentrated to afford tert-butyl 3,6-dihydropyridine-1(2H)-carboxylate, which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846657B2
Source datasetuspto-grants-2014_09
ORD IDord-d9928f5ac42e4e68aa9d83ae7329eae2
Source noteuspto-grants-2014_09