HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butylcyclohexane → HCID 86744722, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butylcyclohexane | HCID 18508 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 19736151 | HCID 19736151 | — |
| Reactant | HCID 78173523 | HCID 78173523 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86744722 | HCID 86744722 | — |
Reaction Steps
4-t-butyl-2-epoxycyclohexane, an intermediate in the synthesis of 4-t-butylhydroxycyclohexyl methacrylate, is prepared by reacting a 4-t-butylcyclohexane with m-chloroperoxybenzoic acid in ethylacetate below 5° C. until mixing is complete, and then at room temperature for two hours. The reaction mixture is washed with aqueous NA2CO3, dried over MgSO4, and filtered. The theoretical reaction is: ##STR20##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05006622 |
| Source dataset | uspto-grants-1991_04 |
| ORD ID | ord-4805c9e53752406f9346b5d54f261c8d |
| Source note | uspto-grants-1991_04 |