69009-34-3

Upstream product

• 69009-26-3 3-(4-Chloro-phenyl)-4-hydroxy-cyclobut-3-ene-1,2-dione 
• 175225-84-0 3-chloro-4-(4-chlorophenyl)-2-hydroxy-2-cyclobuten-1-one 
• 2892-63-9 3,4-Dichlorocyclobut-3-ene-1,2-dione 
• 108-90-7 chlorobenzene 
• 25026-34-0 4-chlorophenacetyl chloride 

Relevant academic research and scientific papers

Synthesis of the substituted 3-cyclobutene-1,2-diones

A convenient synthesis of the novel squaric acid derivatives is reported. Unsymmetrically substituted 3,4-diamino-3-cyclobutene-1,2-diones and 3-amino-4-hydroxy-3-cyclobutene-1,2-diones were prepared by interaction of diethyl squarate with different nucle

Selective 1,4-addition of arenes to 3-chloro-3-cyclobutene-1,2-dione under friedel-crafts conditions. Synthesis and reactivity of 4-aryl-3-chloro-2- hydroxy-2-cyclobuten-1-ones

The reaction of semisquaric chloride (7) with arenes 2 has been investigated. In the presence of 1.1 equiv of AlCl3 and in the temperature range of -15° C to rt the arenes 2a-q afford the 4-aryl-3-chloro-2-hydroxy-2-cyclobuten-1-ones (chloroenols) 8a-q in good yield. By contrast, 7 reacts with 1,4-dimethoxybenzene (2l) in boiling CH 2Cl2 to give a mixture of (2,5-dimethoxyphenyl) cyclobutenedione (9a) (27% yield) and bis(2,5-dimethoxyphenyl)cyclobutenedione (10a) (8% yield). With 1,2,4-trimethoxybenzene (2r) in the presence of trifluoroacetic acid is generated (2,4,5-trimethoxyphenyl)-cyclobutenedione (9b) in 21% yield. The chloroenols 8 allow a series of valuable transformation reactions: with diazomethane the chloroenol methyl ethers 11 are generated, with chlorine the 3-aryl-4-chlorocyclobutenediones 12, and with bromine in MeOH the 3-aryl-4-methoxycyclobutenediones 13. In DMSO or in acetone/H2O the chloroenols 8 eliminate HCl, furnishing the arylcyclobutenediones 14. In a mixture of acetone-d6/D2O/DCl are obtained 4-aryl-cyclobutenediones-3-d 15. For the latter two processes the corresponding 3-aryl-4-chlorocyclobutane-1,2-diones 16 are postulated as intermediates. Thermolysis of the chloroenols 8 and the chloroenol methyl ethers 11 in refluxing m-xylene afforded the 3-chloro-1,2-dihydroxynaphthalenes 17 and the 3-chloro-1-hydroxy-2-methoxynaphthalenes 18, respectively.