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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901556Generated: October 30, 2026

Ammonium formate → Ammonium Hydroxide

https://huagongshe.com/reaction/1901556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-1H-indoleHCID 12050053—
Reactant3-(N-benzyloxycarbonylpiperid-2-ylmethyl)-1H-indoleHCID 19970244—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductAmmonium HydroxideHCID 14923—
ProductIndole, 3-(2-piperidylmethyl)-HCID 21346—
Product3-(pyrrolidin-2-ylmethyl)-1H-indoleHCID 18508996—

Reaction Steps

A mixture of the 3-(N-benzyloxycarbonylpyrrolidin-2-ylmethyl)-1H-indole or the 3-(N-benzyloxycarbonylpiperid-2-ylmethyl)-1H-indole (2.00 mmol), 10% palladium on carbon (0.20 g), and ammonium formate (1.26 g, 20 mmol, 10 eq) in absolute ethanol (15 mL) was stirred under a nitrogen atmosphere for 4 hours. The resulting reaction mixture was filtered through diatomaceous earth, and the filtrate was evaporated under reduced pressure. The residue was column chromatographed using silica gel (approximately 50 g) and slution with a solution of methylene chloride:methanol:ammonium hydroxide [8:2:0.2] or other appropriate solvent system to afford the corresponding 3-(pyrrolidin-2-ylmethyl)-1H-indole or 3-(piperid-2-ylmethyl)-1H-indole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05578612
Source datasetuspto-grants-1996_11
ORD IDord-25f1bc9e0804474882b9bd8e13cb0d0b
Source noteuspto-grants-1996_11