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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217948Generated: November 1, 2026

1,1'-Dimethyl 2,2'-(1,2-diazenediyl)bis(2-methylpropanoate) → HCID 131726986, compound

https://huagongshe.com/reaction/2217948

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-Dimethyl 2,2'-(1,2-diazenediyl)bis(2-methylpropanoate)HCID 75763—
ReactantHCID 23084984HCID 23084984—
ReactantHCID 131726988HCID 131726988—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 131726986HCID 131726986113.1%

Reaction Conditions

Temperature65 °C

Reaction Steps

In a reaction vessel, 133.37 g (0.6 mol) of 3-methoxy-4-(1-ethoxyethoxy)styrene and 119.35 g (0.4 mol) of (tert-butyl)-2,2′-[oxybis(methylene)]bis-2-propenoate were dissolved in 700 ml of tetrahydrofuran. While stirring the resulting solution, a nitrogen gas was passed into the system. Subsequently, 6.91 g (0.03 mol) of polymerization initiator V-601 (produced by Wako Pure Chemical Industries, Ltd.) was added thereto and the reaction solution was heated at 65° C. After stirring under heat for 10 hours by adding V-601 in the same amount as above every one hour, the reaction solution was allowed to cool to room temperature and then added dropwise in 5 L of hexane to precipitate a polymer. The solid obtained by filtration was dissolved in 300 ml of tetrahydrofuran and the resulting solution was again added dropwise in 5 L of hexane. After filtration, the solid obtained was dried under reduced pressure to obtain 209.76 g of a 3-methoxy-4-(1-ethoxyethoxy)styrene/(tert-butyl)-2,2′-[oxybis(methylene)]bis-2-propenoate copolymer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410747B2
Source datasetuspto-grants-2008_08
ORD IDord-907bb9618f2b4183b1b2573528139aea
Source noteuspto-grants-2008_08