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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896438Generated: November 1, 2026

Water → 1-[(2-chloro-1H-indol-1-yl)methyl]-4-propylpyrrolidin-2-one

https://huagongshe.com/reaction/1896438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant2-chloro-1H-indoleHCID 640840—
Reactant1-(Chloromethyl)-4-propylpyrrolidin-2-oneHCID 53629216—
SolventDimethylformamideHCID 6228—
Product1-[(2-chloro-1H-indol-1-yl)methyl]-4-propylpyrrolidin-2-oneHCID 5774301542%

Reaction Conditions

Temperature-20 °C

Reaction Steps

At −78° C., NaH (60% in mineral oil; 220 mg, 5.52 mmol, 1.1 eq) is added to a solution of 2-chloro-1H-indole x160 (0.76 g, 5.02 mmol, 1 eq) in dry DMF (50 ml). The temperature is raised to −20° C. during 20 minutes, then 1-(chloromethyl)-4-propylpyrrolidin-2-one x63 (0.76 g, 5.02 mmol, 1 eq) dissolved in DMF (10 ml) is added drop wise. After 2 hours at room temperature, water (50 ml) is added. The aqueous layer is extracted with CH2Cl2 (3×30 ml). The combined organic layers are dried on anhydrous MgSO4, filtered off and concentrated under reduced pressure to obtain a liquid that is purified on silicagel (AcOEt/Benzine 1/9) yielding 1-[(2-chloro-1H-indol-1-yl)methyl]-4-propylpyrrolidin-2-one 274 as a colorless liquid (605 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518943B2
Source datasetuspto-grants-2013_08
ORD IDord-50e497455e474c4a9f487850217bb754
Source noteuspto-grants-2013_08