HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266885Generated: October 31, 2026
Diethyl Ether → 1-[1-(3,4-Dichlorophenyl)cyclopentyl]ethanone
https://huagongshe.com/reaction/266885
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | 1-(3,4-Dichlorophenyl)cyclopentanecarbonitrile | HCID 21258476 | — |
| Reactant | HCID 178418373 | HCID 178418373 | — |
| Product | 1-[1-(3,4-Dichlorophenyl)cyclopentyl]ethanone | HCID 21258457 | — |
Reaction Steps
Methylmagnesium iodide (3M solution in ether; 100 ml) was added dropwise at 0° C. under nitrogen to a stirred solution of 1-(3,4-dichlorophenyl) cyclopentanecarbonitrile (48 g) in ether (100 ml), then the mixture was stirred at ambient temperature for 24 hours. The resulting solid was collected by filtration, washed with ether, and added in portions to an ice-cold mixture of water (200 ml) and concentrated hydrochloric acid (125 ml). The mixture was heated at 95° C. for 1 hour, then allowed to cool to ambient temperature. The product was extracted into ether (5×100 ml), and the combined extracts were washed with water (2×100 ml), dried over magnesium sulphate, and the solvent removed in vacuo. The residue was distilled to give 1-[1-(3,4-dichlorophenyl)cyclopentyl]ethanone as a pale yellow oil (31.9 g), b.p. 124°-128° C./0.5 mbar.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05652271 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-0f35a9426e714904a682221b0f8c4343 |
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| Source note | uspto-grants-1997_07 |
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