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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1259616Generated: November 1, 2026

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

https://huagongshe.com/reaction/1259616

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 numberUS08466188B2
Source datasetuspto-grants-2013_06
ORD IDord-c7905727e3744155bc0447757dd6feec
Source noteuspto-grants-2013_06