85381-11-9

Upstream product

• 64-17-5 ethanol 
• 835652-06-7 diethyl t-3,c-4-bis(2-hydroxyphenyl)-r-1,t-2-cyclobutanedicarboxylate 

Downstream Products

• 91-64-5 coumarin 
• 5248-12-4 anti head-to-head coumarin dimer 
• 3943-94-0 (E)-ethyl 2-hydroxycinnamate 

Relevant academic research and scientific papers

Thermal Behavior of Head-to-head Coumarin Dimers and Their Lactone-opened Derivatives

The thermal behavior of head-to-head coumarin dimers and twelwe lactone-opened derivatives was investigated.Though the lactone rings in coumarin dimers are very susceptible to nucleophilic ring-opening, heating these derivatives reformed six-membered lactone rings except for certain imide and diamide derivatives.The large neiboring group effect allowed the relactonization by the attack of hydroxyphenyl group to carbonyl carbon in preference to the scission of cyclobutane ring.

Synthesis of Lactone-opened Derivatives of anti and syn Head-to-Head Coumarin Dimers

anti and syn Head-to-head coumarin dimers reacted readily with amines and alcohols to give the corresponding diamides, diesters, imides, or the monoactone derivatives.