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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450578Generated: November 2, 2026

Ammonium formate → HCID 69669353, compound

https://huagongshe.com/reaction/450578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantHCID 69669165HCID 69669165—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 69669353HCID 69669353—

Reaction Steps

Ammonium formate (1.2 g, 19.1 mmol) was added into a suspension of tert-butyl 4-(5-fluoro-2-nitrophenoxy)piperidine-1-carboxylate (2.0 g, 5.8 mmol) and palladium on carbon (5%, 0.4 g) in MeOH (30 mL) at ambient temperature. The solution was stirred for 0.5 hours, filtered through Celite and washed with MeOH. The filtrate was concentrated in vacuo and triturated from diethyl ether to remove the ammonium formate by-products. The sample was purified by flash column chromatography (1:10→1:1 EtOAc/DCM) to yield a colourless oil which crystallised from diethyl ether/petroleum ether (40-60° C.) as a colourless solid (1.6 g, 87%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486953B2
Source datasetuspto-grants-2013_07
ORD IDord-e9a730ca4f7340dfba5b660736f37004
Source noteuspto-grants-2013_07