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 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Acetoxycyclohexene | HCID 11116148 | — |
Reaction Steps
A mixture of 1.100 g of the copper complex of N-salicylidene-3-amino-3-deoxy-1,2-O-isopropylidene-5-O-triphenylmethyl-α-D-ribofuranose, 0.70 g of copper powder, 15 ml of acetonitrile, 5 ml of acetic acid, 15 ml of cyclohexene and 5 of t-butyl peroxybenzoate was stirred at room temperature for 9 hours in a nitrogen atmosphere. After filtering the reaction solution, the filtrate was treated in the same manner as in Example 1 to obtain 1.80 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-afe8e3ceb2824bbf8d1847528e83e154 |
| Source note | uspto-grants-1978_01 |