Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | tert-Butyl peroxybenzoate | HCID 11966 | — |
| Reactant | (S)-(-)-N-salicylidene-1-phenyl-2-(p-tolyl)ethylamine | HCID 136388393 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | 3-Acetoxycyclohexene | HCID 11116148 | — |
Reaction Steps
A mixture of 0.50 g of the copper complex of (S)-(-)-N-salicylidene-1-phenyl-2-(p-tolyl)ethylamine, 0.045 g of copper powder, 25 ml of cyclohexene, 25 ml of acetonitrile, 5 ml of acetic acid and 5 ml of t-butyl peroxybenzoate was heated with stirring at 70° C for 7 hours in a nitrogen atmosphere. After cooling, the reaction mixture was admixed with 50 ml of benzene, washed successively with a 2N aqueous hydrochloric acid solution, water, an aqueous solution saturated with sodium hydrogen carbonate and an aqueous solution saturated with sodium chloride, and dried over anhydrous sodium sulfate. After evaporating the solvent, the residue was distilled under reduced pressure to obtain 1.88 g of 2-cyclohexenyl acetate. B.P. 75°-76° C/21 mmHg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04069385 |
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| Source dataset | uspto-grants-1978_01 |
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| ORD ID | ord-62185435f3b64c9495415c3306017607 |
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| Source note | uspto-grants-1978_01 |
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