HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1287562Generated: October 25, 2026
Hydrogen Peroxide → Diethyl peroxydicarbonate
https://huagongshe.com/reaction/1287562
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Diethyl Pyrocarbonate | HCID 3051 | — |
| Reactant | Vinyl Chloride | HCID 6338 | — |
| Reactant | Peroxide, bis(2-methyl-1-oxopropyl) | HCID 76969 | — |
| Product | Diethyl peroxydicarbonate | HCID 61756 | — |
Reaction Steps
The data of Example III shows that the combined use of isobutyric anhydride and hydrogen peroxide in amounts sufficient to produce theoretically 4.0 × 10-4 moles of diisobutyryl peroxide can initiate the polymerization of vinyl chloride at 50° C. The data further shows that the peroxide is exhausted early in the polymerization. The data of Example IV shows that the combined use of diethyl pyrocarbonate and hydrogen peroxide in amounts sufficient to produce theoretically 3.35 × 10-4 moles of diethyl peroxydicarbonate can initiate the polymerization of vinyl chloride at 50° C. and provide high conversions. Thus, by combining the initiation systems of Examples III and IV as, for example, in Example I (4.5 × 10-4 total moles of theoretical initiator), a smooth and continuous polymerization to high conversions is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US03985720 |
|---|
| Source dataset | uspto-grants-1976_10 |
|---|
| ORD ID | ord-2f24d2dc33f34ec3819d898b1121d255 |
|---|
| Source note | uspto-grants-1976_10 |
|---|