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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115292Generated: October 30, 2026

Ammonium formate → Tert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylate

https://huagongshe.com/reaction/2115292

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactanttert-Butyl 5-benzylhexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylateHCID 4171147—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductTert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylateHCID 414252684%

Reaction Steps

A mixture of compound 4 (130 mg), Pd/C (100 mg, 10%) and ammonium formate (160 mg) in ethanol (10 mL) was heated to reflux for 2 hours and then allowed to cool to room temperature. The solid was filtered off and the filtrate was concentrated in vacuo. The residue was purified by preparative HPLC to provide title compound 5 as a pale yellow oil (76 mg, 84%). LCMS: Rf: 0.371 min, M+H+: 213.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435831B2
Source datasetuspto-grants-2008_10
ORD IDord-cc3d58b5de02434fad6cc75ce0cde871
Source noteuspto-grants-2008_10