HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652196Generated: October 28, 2026
Ethyl Bromide → 4-(2,5-Difluorobenzoyl)-1-methylpiperidine
https://huagongshe.com/reaction/652196
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-chloro-N-methylpiperidine | HCID 79342 | — |
| Reactant | 2,5-Difluorobenzonitrile | HCID 123558 | — |
| Reactant | Ammonium chloride monohydrate | HCID 57429219 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2,5-Difluorobenzoyl)-1-methylpiperidine | HCID 14032495 | 66.5% |
Reaction Steps
To a stirred suspension of Mg (9.62 g, 0.40 moles) in tetrahydrofuran (THF) (45 ml) was added a few ml of bromoethane to initiate the reaction followed by dropwise addition of freshly distilled 4-chloro-N-methylpiperidine (42.3 g, 6.32 moles) in THF (140 ml). The reaction was initiated with a high intensity heat gun and controlled by the rate of addition of the piperidine. After the addition was complete, the reaction was refluxed for 1 hour. Next 2,5-difluorobenzonitrile (48.2 g, 0.318 moles) in THF (20 ml) was added and the reaction was refluxed for an additional 3 hours. The reaction was allowed to stand for 65 hours and was then poured into a solution of NH4Cl/H2O (120 g/400 ml). The mixture was heated on a steam bath for 2 hours, cooled and extracted with ether (500 ml.). Concentration produced an oil (50.6 g) which the product was distilled from (112° C. @ 0.5 mm) to yield 30.4 g (40%) of the product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04670447 |
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| Source dataset | uspto-grants-1987_06 |
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| ORD ID | ord-0a98cee166cd4f268f1e8a7fe8dd09f9 |
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| Source note | uspto-grants-1987_06 |
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