HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 1-(4-Bromo-5-chloro-2-hydroxyphenyl)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 2-Bromo-1-chloro-4-methoxybenzene | HCID 24212081 | — |
| Solvent | Carbon Disulfide | HCID 6348 | — |
| Product | 1-(4-Bromo-5-chloro-2-hydroxyphenyl)ethanone | HCID 59564177 | 99.3% |
Reaction Steps
The 2-bromo-1-chloro-4-methoxybenzene (25.0 g, 113 mmol) [Oakwood cat#035670] was dissolved in carbon disulfide (250 mL), and the acetyl chloride (12 mL, 170 mmol) and aluminum trichloride (37.6 g, 282 mmol) were added. The reaction was heated to reflux and monitored by LC/MS. After heating for 1 h, the reaction became two layers. The reaction allowed to cool to room temperature and poured over ice. The slurry was extracted with ethyl acetate 3×, the combined organic layer was washed with brine, dried over magnesium sulfate and concentrated to give 1-(4-bromo-5-chloro-2-hydroxyphenyl)ethanone as a solid (28.0 g, 99%). 1H NMR (300 MHz, CDCl3) δ 12.12 (s, 1H), 7.78 (s, 1H), 7.31 (s, 1H), 2.62 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09309251B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-f0f7c87820114e84b606c4a4a374221e |
| Source note | uspto-grants-2016_04 |