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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425522Generated: October 30, 2026

Diethyl Ether → 4,7-dichloro-1-pentyl-1H-indole-2,3-dione

https://huagongshe.com/reaction/425522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant1-BromopentaneHCID 8057—
ReactantSodium hydrideHCID 24758—
Reactant4,7-DichloroisatinHCID 2734793—
SolventDimethylformamideHCID 6228—
Product4,7-dichloro-1-pentyl-1H-indole-2,3-dioneHCID 6664266898%

Reaction Steps

To a mixture of sodium hydride (0.17 g, 6.94 mmol, 60% dispersion in mineral oil) in anhydrous N,N-dimethylformamide (5.00 mL) was added a solution of 4,7-dichloro-1H-indole-2,3-dione (1.00 g, 4.60 mmol) in N,N-dimethylformamide (5.00 mL) at 0° C. The brown reaction mixture was stirred for 0.5 h followed by the addition of a solution of 1-bromopentane (0.84 g, 5.55 mmol) in anhydrous N,N-dimethylformamide (5.00 mL). The reaction mixture was stirred at ambient temperature for 16 h and poured into wet ethyl ether (30.0 mL). After the organic layer was separated, it was washed with water (2×20.0 mL), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to dryness. The gummy residue was dried under vacuum and the solid was triturated with ether to give the title compound (0.98 g, 98%): MS (ES+) m/z 286.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106087B2
Source datasetuspto-grants-2012_01
ORD IDord-881d6e49989d46a9afb622e78d1f0458
Source noteuspto-grants-2012_01