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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110862Generated: November 1, 2026

Toluene → 1-(3-Chlorophenyl)-3-(1-benzyl-2-pyrrolidinylidene)-2(1H,3H)-indolone

https://huagongshe.com/reaction/1110862

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant1-Benzyl-3-pyrrolidoneHCID 79176—
Reactant1-(3-Chlorophenyl)-indolin-2-oneHCID 11299530—
SolventDichloromethaneHCID 6344—
Product1-(3-Chlorophenyl)-3-(1-benzyl-2-pyrrolidinylidene)-2(1H,3H)-indoloneHCID 53794442—

Reaction Steps

N-benzyl-2-pyrrolidone (1.58 ml, 9.85 mmoles) was combined with 2 ml toluene under N2 and cooled to 0°-5°. POCl3 (0.5 ml, 5.9 mmoles) was added and the mixture stirred 30 minutes. Toluene (3 ml) and 1-(3-chloro- phenyl-2(1H,3H)-indolone (1.2 g, 4.92 mmoles) were added and the stirred reaction mixture warmed to 25° for 30 minutes and then to 70°-75° for 18 hours. The reaction mixture was cooled, diluted with 100 ml CH2Cl2, washed with saturated NaHCO3, H2O and brine, dried and concentrated in vacuo to an oil (2.6 g). The oil was chromatographed on silica gel (45×150 mm) using CH2Cl2 as eluant, yielding title product, initially an oil which was crystallized from ether/pentane, 1.04 g (53%), m.p. 72°-75°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977178
Source datasetuspto-grants-1990_12
ORD IDord-563af21d5ab64430b657afbf771a5fec
Source noteuspto-grants-1990_12