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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698362Generated: October 31, 2026

1-(Tert-butoxycarbonyl)piperidine-3,5-dicarboxylic acid → Tert-butyl 2,4-dioxo-3-oxa-7-azabicyclo[3.3.1]nonane-7-carboxylate

https://huagongshe.com/reaction/1698362

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Tert-butoxycarbonyl)piperidine-3,5-dicarboxylic acidHCID 23291131—
SolventAcetic AnhydrideHCID 7918—
ProductTert-butyl 2,4-dioxo-3-oxa-7-azabicyclo[3.3.1]nonane-7-carboxylateHCID 59778297—

Reaction Steps

A suspension of piperidine-1,3,5-tricarboxylic acid 1-tert-butyl ester (1 g, 3.6 mmol) in acetic anhydride (20 mL) is heated at reflux for 2 h. The reaction mixture is evaporated 3× times with toluene before it is dried under high vacuum at rt overnight to give a yellow solid. MS (LC-MS): 278 [M+Na]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163773B2
Source datasetuspto-grants-2012_04
ORD IDord-bde663a5bfbe42d6a5ca4c987091a082
Source noteuspto-grants-2012_04