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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-chloro-1H-indole | HCID 640840 | — |
| Reactant | 1-(Chloromethyl)-4-propylpyrrolidin-2-one | HCID 53629216 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[(2-chloro-1H-indol-1-yl)methyl]-4-propylpyrrolidin-2-one | HCID 57743015 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518943B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-50e497455e474c4a9f487850217bb754 |
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| Source note | uspto-grants-2013_08 |
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