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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654522Generated: October 31, 2026

Ammonium formate → tert-Butyl 6-azaspiro[2.5]octan-1-ylcarbamate

https://huagongshe.com/reaction/1654522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantBenzyl 1-{[(tert-butoxy)carbonyl]amino}-6-azaspiro[2.5]octane-6-carboxylateHCID 70347143—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-Butyl 6-azaspiro[2.5]octan-1-ylcarbamateHCID 15282171100%

Reaction Steps

To a solution of the title compound of step 5 (2.2 g, 6.10 mmol) in ethanol (60 ml) was added ammonium formate (1.15 g, 18.3 mmol) followed by palladium on activated carbon (10% palladium content, 1.94 g, 1.83 mmol). The mixture was stirred at room temperature for 1 hour. The reaction mixture was filtered, and the filtrate was concentrated in vacuo to afford the title compound as a white foam (1.4 g, 6.1 mmol, yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05407943
Source datasetuspto-grants-1995_04
ORD IDord-694bdfe2edc745578daaf95a74bc4271
Source noteuspto-grants-1995_04