Vashisth, N.; Sharma, S. P.; Kumar, S.; Aruna published the artcile< One-Pot Green Synthesis of 2-Hydroxybenzoyl(cinnamoyl)methanes and 2-Styrylchromones Using Dual-Frequency Ultrasonication>, Synthetic Route of 17082-09-6, the main research area is styrylchromone preparation green chem ultrasound; hydroxybenzoyl cinnamoyl methane preparation heterocyclization; hydroxyacetophenone cinnamoyl chloride ultrasonication Baker Venkataraman rearrangement.
One-pot green synthesis of (2-hydroxybenzoyl)(cinnamoyl)methanes (E)-I (R1 = H, OMe; R2 = H, Me; R3 = H, OMe) has been performed by reacting 2-hydroxyacetophenones 2-OH-4-R1-5-R2C6H2C(O)CH3 with cinnamoyl chlorides (E)-4-R3C6H4CH=CHC(O)Cl using activated Ba(OH)2, followed by Baker-Venkataraman rearrangement assisted by dual-frequency ultrasonication. Cyclization of (2-hydroxybenzoyl)(cinnamoyl)methanes I using methanesulfonic acid along with dual-frequency ultrasound irradiation resulted in the formation of 2-strylchromones (E)-II in a single step.
Russian Journal of Organic Chemistry published new progress about Alkyl aryl ketones Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 17082-09-6 belongs to class chlorides-buliding-blocks, and the molecular formula is C9H7ClO, Synthetic Route of 17082-09-6.
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics