839721-38-9

Basic information

• Product Name: Benzene, 1-(1-butoxyethenyl)-2-fluoro-
• CAS NO: 839721-38-9
• Molecular Formula: C12H15FO
• Molecular Weight: 194.249
• Mol File: 839721-38-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 1-(1-butoxyethenyl)-2-fluoro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-(1-butoxyethenyl)-2-fluoro-(839721-38-9)
• EPA Substance Registry System: Benzene, 1-(1-butoxyethenyl)-2-fluoro-(839721-38-9)

Safety Data

• Hazardous Substances Data: 839721-38-9(Hazardous Substances Data)

Upstream product

• 1072-85-1 o-fluorobromobenzene 
• 111-34-2 -butyl vinyl ether 
• 1993-03-9 o-fluorophenylboronic acid 

Downstream Products

• 445-27-2 2'-Fluoroacetophenone 

Relevant articles and documents

Efficient synthesis of alkyl aryl ketones & ketals via palladium-catalyzed regioselective arylation of vinyl ethers

The combination of Pd(OAc)2 with 1,3-bis(diphenylphosphino) propane (dppp) in ethylene glycol constitutes a high-performance catalytic system for highly regioselective arylation of a range of electron-rich vinyl ethers by aryl bromides to provide, upon hydrolysis, alkyl aryl ketones and cyclic ketals in good yields with up to 3.75 × 105 TON and 15625 h-1 TOF.

Hydrogen-bond-directed catalysis: Faster, regioselective and cleaner heck arylation of electron-rich olefins in alcohols

A general method for the regioselective Heck reaction of electronrich olefins is presented. Fast, highly regioselective Pd-catalysed α-arylation of electron-rich olefins, vinyl ethers (1a-d), hydroxyl vinyl ethers (1e,f), enamides (1g,h) and a substituted vinyl ether (1i) has been accomplished with a diverse range of aryl bromides (2a-r), for the first time, in cheap, green and easily available alcohols with no need for any halide scavengers or salt additives. The reaction proceeds with high efficiency, leading exclusively to the a-products, in 2-propanol and particularly in ethylene glycol. In the latter, the arylation can be catalysed at a palladium loading of 0.1 mol% and finish in as short a time as 0.5 h. The remarkable performance of the alcohol solvents in promoting a regiocontrol is attributed to their hydrogen-bond- donating capability, which is believed to facilitate the dissociation of halide anions from PdII, and hence, the generation of a key ionic Pd II-olefin intermediate responsible for the a product. This belief is further strengthened by the study of a benchmark arylation reaction in 21 different solvents. The study revealed that exclusive α-regioselective arylation takes place in almost all of the protic solvents, and there is a rough correlation between the α-arylation rates and the solvent parameter ETN. The method is simpler, cleaner and more general than those established thus far.