Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479029Generated: October 26, 2026

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

https://huagongshe.com/reaction/479029

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) δ6.25 (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 numberUS06642398B2
Source datasetuspto-grants-2003_11
ORD IDord-32acf88633b2448ea5bce38b86f94078
Source noteuspto-grants-2003_11