n-Butyllithium C 4 H 9 Li (abbreviated n-BuLi) is an organolithium reagent. It is widely used as a polymerization initiator in the production of elastomers such as polybutadiene or styrene …

Sep 6, 2019 · Butyllithium reacts with some organic bromides and iodides in an exchange reaction to form the corresponding organolithium derivative. The reaction usually fails with organic …

The reaction of n-BuLi with THF produces the enolate of acetaldehyde, which is difficult to form cleanly by direct deprotonation of acetaldehyde. Reaction of n -butyllithium with ethers

n-BuLi is a strong base (pKa ~ 50) and is typically sold as a solution in hexanes (1.6M or 2.5M). It reacts violently with water and needs to be stored under an inert atmosphere to prevent its …

the syringe and immediately suspected a pyrophoric reaction was taking placed from leaked n-BuLi. They reacted quickly, doffing their glove properly, grabbing it by the palm and inverting it …

Sep 5, 2022 · tert-Butyllithium solution (tert-BuLi) is an organolithium compound, used as a strong base in organic chemistry. It facilitates lithium-halogen exchange reaction and also can be …

Using n-BuLi in dry THF or ether at -78 degrees under a nitrogen atmosphere, I'm trying to lithiate the thiophene moiety and then further react it with octafluorocyclopentene (injected directly...

BuLi forms a weaker complex with LiCl, so that the reaction of BuCl with Li produces a precipitate of LiCl. Butyllithium is a strong base, but it is also a powerful nucleophile and reductant, …

Jun 2, 1975 · In summary, the reaction of butyllithium with TEMPO. (and with other nitroxyl radicals examined) provides a rapid method of converting the radical to diamagnetic

Jun 24, 2024 · n-Butyllithium (n-BuLi), with a molecular formula C4H9Li and a molecular weight of 64.05, is a widely utilized organolithium reagent of significant importance in organic synthesis. …