Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2295758Generated: October 30, 2026

Diethyl Ether → N-propionyl-3-(3-methoxyphenyl)pyrrolidone

https://huagongshe.com/reaction/2295758

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriethylamineHCID 8471—
ReactantPropionyl chlorideHCID 62324—
Reactant3-(3-Methoxyphenyl)pyrrolidineHCID 12937991—
ProductN-propionyl-3-(3-methoxyphenyl)pyrrolidoneHCID 23045623100%

Reaction Conditions

Temperature0 °C

Reaction Steps

3-(3-Methoxyphenyl)pyrrolidine (8.86 g, 0.050 mol) and triethylamine (5.57 g, 0.055 mol) was dissolved in 500 ml of dry ether. The solution was cooled to 0° C. and propionyl chloride (5.09 g, 0.055 mol) was added dropwise with stirring. The reaction mixture was then allowed to acquire ambient temperature, whereafter it was refluxed for 30 minutes. Triethylamine hydrochloride was filtered off, and the filtrate was evaporated leaving 11.7 g (100%) of crude N-propionyl-3-(3-methoxyphenyl)pyrrolidone, which was used in the next reaction step without further purification. The crude amide (11.7 g, 0.050 mol) was reduced with LiAlH4 (2.85 g, 0.075 mol) in refluxing ether (200 ml) for 24 hours. Work-up of the reaction mixture afforded 10 g of product, which upon distillation in vacuo yielded 9.1 g ((83%) of N-propyl-3-(3-methoxyphenyl)-pyrrolidone b.p. 85°-86° C./0.1 mm Hg. MS: m/e 219 (M+, 12%) 190 (M--C2H5, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04426386
Source datasetuspto-grants-1984_01
ORD IDord-6963eec29b614d23b07f4dc10aa8a2c2
Source noteuspto-grants-1984_01