Purchase CAS:1514-82-5,view related peer-reviewed papers,technical documents,similar products,MSDS & more. 2-Bromo-3,3,3-trifluoroprop-1-ene (also referred to as 2-BTP) is an organic compound belonging to the class of halogenated hydrocarbons. It is a colorless liquid with a sweet, pungent odor and a boiling point of 115°C. 2-BTP has been used in various scientific research applications due to its unique properties, such as...
2-Bromo-3,3,3-trifluoroprop-1-ene (also referred to as 2-BTP) is an organic compound belonging to the class of halogenated hydrocarbons. It is a colorless liquid with a sweet, pungent odor and a boiling point of 115°C. 2-BTP has been used in various scientific research applications due to its unique properties, such as its low vapor pressure, low solubility in water, and high stability.
Scientific Research Applications
Synthesis of α-(Trifluoromethyl)styrenes: This compound is utilized in the generation of thermally unstable vinyllithium by lithiation, which then undergoes borylation in a flow microreactor system. The resultant vinylborate is directly used for the Suzuki–Miyaura coupling, yielding α-(trifluoromethyl)styrenes in high yields (Fujita et al., 2018).
Syntheses of CF3-Containing Allylic Alcohols and Amines: It involves a rapid lithium-halogen-exchange reaction, generating vinyllithium which reacts with more reactive electrophiles to afford 2-(trifluoromethyl)allyl alcohols and N-[2-(trifluoromethyl)allyl] sulfoamides. This methodology allows for the synthesis of various CF3-containing compounds, which have significance in medicinal chemistry (Nadano et al., 2010).
Preparation of 3,3,3-Trifluoropropene Oxide (TFPO): This compound is used in the bromination of 3,3,3-trifluoropropene followed by treatment with acetic acid to produce 2-bromo-3,3,3-trifluoropropyl acetate, which on further processing yields TFPO (Ramachandran & Padiya, 2007).
Photocatalytic Reactions: 2-Bromo-3,3,3-trifluoropropene has been employed as a coupling partner in photocatalytic defluorinative reactions, leading to the formation of various difluoromethylidene-tetrahydroquinolines (Zeng et al., 2022).
Electrochemical Carboxylation: It's involved in electrochemical carboxylation processes that lead to the efficient fixation of carbon dioxide, yielding corresponding 2-aryl-3,3,3-trifluoropropanoic acids. This method has been applied to synthesize β,β,β-trifluorinated non-steroidal anti-inflammatory drugs (Yamauchi, Hara & Senboku, 2010).