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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1188160Generated: November 4, 2026

Ammonium formate → 3-(3,5-Difluorophenyl)-3-methoxypyrrolidine

https://huagongshe.com/reaction/1188160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant1-Benzyl-3-(3,5-difluorophenyl)-3-methoxypyrrolidineHCID 19935849—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product3-(3,5-Difluorophenyl)-3-methoxypyrrolidineHCID 1993587479.8%

Reaction Steps

A mixture of (−)-1-benzyl-3-(3,5-difluorophenyl)-3-methoxypyrrolidine (0.43 g, 1.41 mmol), mlammoniumformate (0.18 g, 2.83 mmol) and palladium on carbon (10%, 0.08 g) in ethanol (10 ml), was refluxed for 40 min. Additional ammoniumformate (0.18 g, 2.83 mmol) was added and after 90 min reflux all starting material was consumed. The reaction mixture was allowed to reach ambient temperature and filtrated over a pad of celite and the solvent was evaporated. The remaining oil was dissolved in methylen chloride and potassium carbonate (2 g), was added. The mixture was stirred over night, filtrated and evaporated to give the title compound (0.24 g, 79%). [a]D=−2.1° (methanol). The amine was converted to the oxalic acid salt and recrystallized from methanol/diethyl ether: M.p. 185-187° C. MS m/z (rel. intensity, 70 eV) 213 (M+, 1), 198 (58), 183 (bp), 171 (84), 141 (55).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673962B2
Source datasetuspto-grants-2014_03
ORD IDord-18d05e950b67454dbb23616fb47d9675
Source noteuspto-grants-2014_03