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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258219Generated: October 31, 2026

Isoprene → HCID 19842620, compound

https://huagongshe.com/reaction/258219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopreneHCID 6557—
ReactantStyreneHCID 7501—
Reactant2-Methylbuta-1,3-diene;styreneHCID 159989—
ReactantCID 53628100HCID 178418400—
SolventCyclohexaneHCID 8078—
ProductHCID 19842620HCID 19842620—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a 2.6 liter autoclave were charged 1900 ml of cyclohexane and 88.1 gm of styrene monomer. The mixture was heated to 60° C. and 3.7 ml of a 1.4 molar solution of sec-butyllithium initiator in cyclohexane was added. After 40 minutes, when analysis of the reaction mixture indicated that polymerization of the styrene monomer was complete, the reaction temperature was reduced to 50° C., and 116.7 gm of isoprene was added. After 45 minutes, no unreacted isoprene was detected. The living styrene-isoprene diblock polymer was then coupled to form a styrene-isoprene-styrene triblock polymer by adding 32.0 ml of 0.12M 1,2-dibromoethane in cyclohexane over a period of 11 minutes. Analysis of the product by gel-permeation chromatography (GPC) indicated that the triblock polymer had a peak molecular weight of 76,800, and contained approximately 12% residual diblock. From the proton NMR spectrum of the product, it was determined that it contained 41.7 wt. % styrene. The solvent was removed from the polymer solution under vacuum at 90° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05266394
Source datasetuspto-grants-1993_11
ORD IDord-021125ec015a4eba933b5cf5f3a0bc85
Source noteuspto-grants-1993_11