Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 536582Generated: October 25, 2026

Diazomethane → 6-(tert-butoxycarbonyl)-6-azaspiro[2.5]octane-5(S)-carboxylic acid benzyl ester

https://huagongshe.com/reaction/536582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiazomethaneHCID 9550—
Reactant4-methylene-1-(tert-butoxycarbonyl)piperidine-2(S)-carboxylic acid benzyl esterHCID 66848724—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product6-(tert-butoxycarbonyl)-6-azaspiro[2.5]octane-5(S)-carboxylic acid benzyl esterHCID 6684836888%

Reaction Steps

To a solution of (S)-4-methylene-piperidine-1,2-dicarboxylic acid 2-benzyl ester 1-tert-butyl ester (intermediate 15 prepared by Method A, 120 g, 0.36 mol) in anhydrous THF (1 L) was added diazomethane in ether (500 ml) [which was prepared from methyl-3-nitro-1-nitroxoguanide (213 g) in 40% KOH (1 L)] at −25° C. to −35° C. slowly under the protection of nitrogen and warmed to room temperature slowly (about 4 hours) and stirred at room temperature for 10 hours. The mixture is filtered and the liquid phase was evaporated to obtain a crude that was purified by silica gel chromatography (petroleum ether/ethyl acetate from 10/1 to 5/1). (S)-6-Aza-spiro[2.5]octane-5,6-dicarboxylic acid 5-benzyl ester 6-tert-butyl ester was obtained as colourless oil (110 g), yield:88%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859608B2
Source datasetuspto-grants-2014_10
ORD IDord-ff08b30816834a1aa2c3edf551fe5a1f
Source noteuspto-grants-2014_10