HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1499721Generated: October 30, 2026
1-(3-Bromo-5-chloro-2-hydroxy-4-methylphenyl)ethanone → 3-Acetyl-5-chloro-2-hydroxy-6-methylbenzonitrile
https://huagongshe.com/reaction/1499721
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(3-Bromo-5-chloro-2-hydroxy-4-methylphenyl)ethanone | HCID 12027479 | — |
| Reactant | HCID 178418260 | HCID 178418260 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 3-Acetyl-5-chloro-2-hydroxy-6-methylbenzonitrile | HCID 58368516 | — |
Reaction Steps
A mixture of 1-(3-bromo-5-chloro-2-hydroxy-4-methylphenyl)ethanone (4.85 g, 18.4 mmol) and copper cyanide (2.47 g, 27.6 mmol) in N-methylpyrrolidinone (15 mL) was heated at 200° C. for 1 h. After cooled to rt, the mixture was diluted with EtOAc and 1 N HCl. The layers were separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with water, then brine and dried over magnesium sulfate, then concentrated to dry under reduced pressure. The residue was used directly in next step (3.7 g, 96%). LCMS calculated for C10H9ClNO2 (M+H)+: m/z=210.0; Found: 210.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09199982B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-e8510ea7f3e140e1aaafa95a34f28f58 |
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| Source note | uspto-grants-2015_12 |
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