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Hydrogen Peroxide → Diethyl peroxydicarbonate

HRID 1287562
Notes
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Reaction equation

HRID 1287562 reaction equation
[CH:1](Cl)=[CH2:2].C(O[O:10][C:11](=[O:15])C(C)C)(=O)C(C)C.C([O:21][C:22]([O:24][CH2:25][CH3:26])=[O:23])(=O)OCC.[OH:27]O>>[C:22]([O:21][O:10][C:11]([O:15][CH2:1][CH3:2])=[O:27])([O:24][CH2:25][CH3:26])=[O:23]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 4

HCID 784Hydrogen PeroxideHCID 3051Diethyl PyrocarbonateHCID 6338Vinyl ChlorideHCID 76969Peroxide, bis(2-methyl-1-oxopropyl)

Product 1

HCID 61756Diethyl peroxydicarbonate

Procedure

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.

Workup

  1. customis exhausted early in the polymerization

Sources & evidence

ORD record
ord-2f24d2dc33f34ec3819d898b1121d255
Source dataset
uspto-grants-1976_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US03985720

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes