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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441109Generated: November 3, 2026

Allyl bromide → Isoprene butadiene

https://huagongshe.com/reaction/1441109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1,3-ButadieneHCID 7845—
Reactant1,4-ButanediolHCID 8064—
ReactantNeodymiumHCID 23934—
ReactantButanediolHCID 165788—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantHCID 86749369HCID 86749369—
ReactantHCID 131719348HCID 131719348—
CatalystNeodymiumHCID 23934—
SolventHexaneHCID 8058—
ProductIsoprene butadieneHCID 16828887%

Reaction Conditions

Temperature20 °C

Reaction Steps

In this experiment, an isoprene-butadiene copolymer was synthesized using an alcohol modified neodymium catalyst system modified with 1,4-butanediol. In this procedure, a one gallon (3.78 liter) reactor was charged with 1,093 grams of hexane containing 81.9 grams of butadiene and 663 grams of 1.2 molar diisobutylaluminum hydride (DIBAH) in hexane (i.e., 25% weight percent DIBAH). To this solution was then added 6.78 grams of 1,4-butanediol with stirring and with temperatures maintained at 20° C. The suspension of the butanediol gradually dissolved upon reacting with the DIBAH. After one hour of stirring, 105.4 grams of a 10.3% neodymium solution (neodymium neodecanoate), diluted with 165 grams of hexane, was added to the reactor. The solution was stirred for another thirty minutes after which time. 19.1 grams of allyl bromide was added. The cooling was stopped and the mixture allowed to warmup to ambient (and above) temperature. After the exotherm subsided, the catalyst solution was aged by heating at 65° C. for ninety minutes. The catalyst prepared had a butanediol-DIBAH!-ND-allyl bromide-butadiene molar component ratio of 1-16!-1-2-20, respectively, and a concentration of 0.025 molarity with respect to the neodymium. The aged catalyst was then cooled and stored in a dry container under nitrogen.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05502126
Source datasetuspto-grants-1996_03
ORD IDord-d8743bbfa9534f1fba023f767dd24ce4
Source noteuspto-grants-1996_03