HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicumyl peroxide → Dicumyl peroxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicumyl peroxide | HCID 6641 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Hexahydrophthalic anhydride, cis- | HCID 641660 | — |
| Reactant | Cumen hydroperoxide | HCID 53627471 | — |
| Product | Dicumyl peroxide | HCID 6641 | — |
| Product | cis-1,2-Cyclohexanedicarboxylic acid | HCID 245564 | — |
Reaction Steps
The reaction described in Example 2 was repeated with 14.7 gm (95 millimoles) cis-1,2-cyclohexanedicarboxylic anhydride substituted for the acetic anhydride. After a total reaction time of 125 minutes (at 18°±1° C.), 9.9% of the cumene hydroperoxide remained unreacted. The reaction was quenched (sodium acetate) after a total time of 245 minutes and, after recovery in a manner similar to Example 2, afforded 35.9 gm crude product which contained about 70% dicumyl peroxide. (An approximate value for dicumyl peroxide was obtained in this case because the elution of cis-1,2-cyclohexanedicarboxylic acid on the gas-liquid chromatography column partially overlapped with the dicumyl peroxide).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04198528 |
| Source dataset | uspto-grants-1980_04 |
| ORD ID | ord-20550b7b99494ce5a3c05aff23536c38 |
| Source note | uspto-grants-1980_04 |