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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167900Generated: November 2, 2026

Ammonia → 4-(2-Methyl-pentyl)-pyrrolidin-2-one

https://huagongshe.com/reaction/1167900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodiumHCID 5360545—
Reactant1-Benzyl-4-(2-methyl-pentyl)-pyrrolidin-2-oneHCID 21888233—
SolventTetrahydrofuranHCID 8028—
Product4-(2-Methyl-pentyl)-pyrrolidin-2-oneHCID 2188817492.6%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 250 mL 3-neck flask equipped with a dry ice condenser was chilled to −78° C. Ammonia (80 mL) was condensed into the flask and 1-benzyl-4-(2-methyl-pentyl)-pyrrolidin-2-one 76 (1.67 g, 0.006 mol) in 15 mL THF was added. Freshly cut sodium beads were added until a deep blue color persisted. The cooling bath was removed and the reaction stirred at reflux (−33° C.) for 1 hour. The reaction was quenched with ammonium chloride and the excess ammonia was allowed to evaporate. The resulting residue was diluted with water, extracted with dichloromethane, and dried over magnesium sulfate. Evaporation of the solvent followed by chromatography on silica eluting with 1:1 acetone/hexane gave 0.94 g, 86% of the 4-(2-Methyl-pentyl)-pyrrolidin-2-one 77. 1H NMR (CDCl3) δ 6.25 (br, 1H), 3.44 (m, 1H), 2.95 (m, 1H), 2.54 (m, 1H), 2.40 (m, 1H), 1.98 (m, 1H), 1.30 (m, 6H), 0.80 (m, 6H). MS, m/z (relative intensity): 212 [M+2H+CH3CN, 100%], 171 [M+2H, 72%], 170 [M+1H, 65%].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06620829B2
Source datasetuspto-grants-2003_09
ORD IDord-1864ee88e0e94e17ba917164c63f006b
Source noteuspto-grants-2003_09