HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192587Generated: October 31, 2026
1-(3-Bromo-5-chloro-2-hydroxy-4-methylphenyl)ethanone → 3-Acetyl-5-chloro-2-hydroxy-6-methylbenzonitrile
https://huagongshe.com/reaction/1192587
Participants
| Role | Name | HCID | Charge |
|---|
| 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 hour. After cooling to room temperature, the mixture was diluted with ethyl acetate and 1 N HCl. The layers were separated and the aqeous layer was extracted with ethyl acetate. The combined organic layers were washed with water, then brine and dried over magnesium sulfate. After concentration to dryness under reduced pressure, the residue was used directly in the 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 |
|---|
| Patent number | US08680108B2 |
|---|
| Source dataset | uspto-grants-2014_03 |
|---|
| ORD ID | ord-be56b57f80334838ad3558dd0755118b |
|---|
| Source note | uspto-grants-2014_03 |
|---|