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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859841Generated: October 26, 2026

Allyl bromide → Isoprene butadiene

https://huagongshe.com/reaction/859841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1,3-ButadieneHCID 7845—
Reactant1,4-ButanediolHCID 8064—
ReactantNeodymiumHCID 23934—
ReactantButanediolHCID 165788—
ReactantDiisobutylaluminumhydrideHCID 21225700—
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 warm up 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 numberUS07153805B2
Source datasetuspto-grants-2006_12
ORD IDord-1b5e7d4c63d649a5acc6f2f31a7f77e5
Source noteuspto-grants-2006_12