HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645065Generated: October 29, 2026
Diethyl Ether → 4,7-dichloro-1-pentyl-1H-indole-2,3-dione
https://huagongshe.com/reaction/645065
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1-Bromopentane | HCID 8057 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4,7-Dichloroisatin | HCID 2734793 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4,7-dichloro-1-pentyl-1H-indole-2,3-dione | HCID 66642668 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700641B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-646f4dbbbfa44212a19e22887f8e6880 |
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| Source note | uspto-grants-2010_04 |
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