HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → 3-Acetoxycyclohexene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Reactant | tert-Butyl peroxybenzoate | HCID 11966 | — |
| Reactant | (S)-(+)-N-salicylidene-1-phenylethylamine | HCID 135405060 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Acetoxycyclohexene | HCID 11116148 | — |
Reaction Steps
A mixture of 0.451 g of (S)-(+)-N-salicylidene-1-phenylethylamine, 0.182 g of cupric acetate, 0.7 g of copper powder, 15 ml of cyclohexene, 15 ml of acetonitrile, 5 ml of acetic acid and 5 ml of t-butyl peroxybenzoate was stirred at 20° to 25° C for 6.5 hours in a nitrogen atmosphere. After the reaction, the reaction mixture was treated in the same manner as in Example 1 to obtain 1.60 g of 2-cyclohexenyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04069385 |
| Source dataset | uspto-grants-1978_01 |
| ORD ID | ord-d1d2dbc790ea40f888fd8db2c8af8397 |
| Source note | uspto-grants-1978_01 |