HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Acetylhydroquinone → 5'-(6-Chlorohexoxy)-2'-hydroxyacetophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Acetylhydroquinone | HCID 10279 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Bromo-6-chlorohexane | HCID 80516 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 5'-(6-Chlorohexoxy)-2'-hydroxyacetophenone | HCID 14983094 | 83.2% |
Reaction Steps
A mixture of 2',5'-dihydroxyacetophenone (150 g), 1-bromo-6-chlorohexane (186 g), and potassium carbonate (186 g) in 2500 mL of 2-butanone was refluxed for 16 hours. The solvent was removed in vacuo and the residue was stirred with 1000 mL of methylene chloride. After filtration, the filtrate was washed with 10% KOH (250 mL), water (250 mL), and brine (250 mL). The solution was dried over magnesium sulfate and the solvent was removed to give an oil which solidified overnight to give 210 g of 5'-(6-chlorohexoxy)-2'-hydroxyacetophenone as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05359098 |
| Source dataset | uspto-grants-1994_10 |
| ORD ID | ord-22682c8c6c4045129131db0e0d1a4c15 |
| Source note | uspto-grants-1994_10 |