Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | Fluorobenzene | HCID 10008 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Product | HCID 15047101 | HCID 15047101 | 30% |
Reaction Steps
To a fluorobenzene (5 mL) solution of cyclohexene (82 mg, 1 mmol) at RT was added acetyl chloride (86 mg, 1.1 mmol) and then the reaction was cooled in an ice bath. Aluminum chloride (150 mg, 1.1 mmol) was slowly added to the solution, then the reaction was slowly allowed to warm to room temperature, was stirred at room temperature for 24 h and was then heated to 80° C. for 1 h. The reaction mixture was cooled to room temperature and was then slowly added to ice cold water. The mixture was extracted with ethyl acetate and the organic portion was dried over sodium sulfate, concentrated under vacuum, and purified on a silica gel column to afford 1-[4-(4-fluoro-phenyl)-cyclohexyl]-ethanone containing about 30% of another unidentified substance (176 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08563742B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-bcbc5358a4474d19a698253c2c3e52b7 |
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| Source note | uspto-grants-2013_10 |
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