HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087715Generated: November 1, 2026
Hydrochloric Acid → 3-(2-Methoxybenzoyl)benzonitrile
https://huagongshe.com/reaction/1087715
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Iodine | HCID 807 | — |
| Reactant | 2-Bromoanisole | HCID 11358 | — |
| Reactant | 3-Cyanobenzoyl chloride | HCID 308483 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(2-Methoxybenzoyl)benzonitrile | HCID 15718533 | 80% |
Reaction Steps
30 g (0.16 mol) of 2-bromoanisole are added dropwise to a mixture of 3.85 g (0.16 mol) of magnesium, containing a crystal of iodine, in 75 ml of anhydrous tetrahydrofuran and the reaction mixture is then refluxed for 1 hour. The resulting solution is then added dropwise to a solution of 26.48 g (0.16 mol) of 3-cyanobenzoyl chloride in 75 ml of anhydrous tetrahydrofuran, cooled to -75° C. The temperature is allowed to rise to 20° C., the reaction medium is hydrolyzed with a 1N aqueous solution of hydrochloric acid and the expected product is then extracted with ethyl acetate. The organic phase obtained is washed with water, dried over magnesium sulfate and then evaporated under reduced pressure. 30 g of the expected product (yield: 80%) are obtained in the form of crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04960758 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-c6caa68a70fd4db3b92c9fa4ade70935 |
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| Source note | uspto-grants-1990_10 |
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