HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenetole → Cyclopropyl 4-ethoxyphenyl ketone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenetole | HCID 7674 | — |
| Reactant | Cyclopropanecarbonyl chloride | HCID 77637 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | Cyclopropyl 4-ethoxyphenyl ketone | HCID 3449314 | — |
Reaction Steps
Alternatively, the substituted-phenyl cyclopropyl ketones may be prepared by reacting cyclopropanecarboxylic acid chloride with an appropriately substituted-phenyl compound in the presence of a Friedel-Crafts catalyst, e.g., aluminum chloride. In Example 6, Step A, cyclopropanecarboxylic acid chloride is reacted with ethoxybenzene in the presence of aluminum chloride, yielding cyclopropyl (4-ethoxyphenyl) ketone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04808762 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-160afd0f4af840c0b5b384fbb2716072 |
| Source note | uspto-grants-1989_02 |