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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039307Generated: October 31, 2026

Isoprene → HCID 19842620, compound

https://huagongshe.com/reaction/2039307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopreneHCID 6557—
ReactantStyreneHCID 7501—
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantTetramethoxysilaneHCID 12682—
ReactantButyllithiumHCID 178418339—
SolventCyclohexaneHCID 8078—
ProductHCID 19842620HCID 19842620—

Reaction Conditions

Temperature40 °C

Reaction Steps

To a pressure-resistant reactor, 23.3 kg of cyclohexane, 2.6 millimoles of TMEDA and 1.90 kg of styrene were added and stirred at 40° C. Added thereto was 172.9 millimoles of n-butyl lithium, and while the temperature was increased to 50° C., the mixture was polymerized for 1 hour. The degree of polymerization conversion of styrene was 100%. Subsequently, 8.10 kg of isoprene was added to the reactor continuously over 1 hour while the temperature was controlled to maintain 50 to 60° C. After the addition of isoprene was completed, the polymerization was performed for additional 1 hour. The degree of polymerization conversion of isoprene was 100%. Subsequently, 34.5 millimoles of tetramethoxysilane was added as a coupling agent and the coupling reaction was performed for 2 hours to form a branched styrene-isoprene-styrene block copolymer, which would be the block copolymer B. After that, 344.8 millimoles of methanol was added as a polymerization terminator to the solution in which the styrene-isoprene block copolymer having an active terminal remained and mixed well to terminate the reaction. Part of the reaction solution obtained was extracted and subjected to the same measurements as Preparation example 1. The values thereof are shown in Table 2. Subsequent treatments that were the same as those of Preparation example 1 were carried out to recover the block copolymer composition of Preparation example 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08578852B2
Source datasetuspto-grants-2013_11
ORD IDord-f1c47158ea864473b365f8088cb7232d
Source noteuspto-grants-2013_11