HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 368968Generated: October 30, 2026
Hydrochloric Acid → 2-Chloro-3-(3-chlorobenzoyl)-6-ethylpyridine
https://huagongshe.com/reaction/368968
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Bromo-3-chlorobenzene | HCID 7928 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 2-Chloro-6-ethylnicotinonitrile | HCID 21930433 | — |
| Product | 2-Chloro-3-(3-chlorobenzoyl)-6-ethylpyridine | HCID 23284489 | 22% |
Reaction Steps
Magnesium (2.72 g, 112 mmol) was added to a tetrahydrofuran (200 ml) solution of 3-bromochlorobenzene (22.1 g, 115 mmol), and the mixture was stirred at room temperature. Since spontaneous exothermic reaction occurred, the stirring was continued until the exothermicity was ceased. The reaction solution was cooled to -20° C., mixed with 2-chloro-3-cyano-6-ethylpyridine (9.33 g, 56 mmol) and then stirred for 16 hours at room temperature. The reaction solution was mixed with saturated ammonium chloride aqueous solution and stirred for 30 minutes at room temperature and then mixed with 1 N hydrochloric acid and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, magnesium-sulfate was removed by filtration and then the filtrate was concentrated under a reduced pressure. Thereafter, the resulting residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give 2-chloro-3-(3-chlorobenzoyl)-6-ethylpyridine (3.48 g, 22%) as a pale yellow oily material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06136810 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-dde86781619949e4b9cc33ec682b99d2 |
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| Source note | uspto-grants-2000_10 |
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