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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489122Generated: October 30, 2026

Isoprene → Styrene

https://huagongshe.com/reaction/489122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopreneHCID 6557—
ReactantStyreneHCID 7501—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantCID 53628100HCID 178418400—
SolventCyclohexaneHCID 8078—
ProductStyreneHCID 7501—
ProductHCID 19842620HCID 19842620—

Reaction Steps

In a pressure vessel where dry nitrogen had been substituted, styrene was polymerized at 60° C. in cyclohexane as a solvent in the presence of s-butyllithium as a polymerization initiator, and then TMEDA was added as a Lewis base. Then, isoprene and styrene were consecutively polymerized to give a styrene-isoprene-styrene block copolymer. The thus-obtained block copolymer was hydrogenated in cyclohexane in the presence of Pd/C as a catalyst under a 2 MPa hydrogen atmosphere, to give a hydrogenated block copolymer (the hydrogenated block copolymer obtained in Referential Example 2 will be abbreviated as “Copolymer No. 1” hereinafter). Table 3 shows a styrene content, a number average molecular weight, a vinyl bond content and a hydrogenation ratio of the obtained Copolymer No. 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06977105B1
Source datasetuspto-grants-2005_12
ORD IDord-e7f8d6354c674b08a7acfba0ec169268
Source noteuspto-grants-2005_12