4364-36-7

Upstream product

• 99-61-6 3-nitro-benzaldehyde 
• 80918-89-4 (2,7-dichlorofluorenylidene)triphenylphosphorane 
• 82764-09-8 2,7-Dichlorofluorenylidenetriphenylarsenane 
• 6297-11-6 2,7-dichlorofluorenone 
• 82764-08-7 2,7-Dichlorofluorenyltriphenylarsonium bromide 
• 80918-70-3 (2,7-dichlorofluorenyl)triphenylphosphonium bromide 
• 7012-18-2 9-bromo-2,7-dichlorofluorene 
• 110138-01-7 dimethyl 2,7-dichloro-9-fluorenylphosphonate 

Relevant academic research and scientific papers

Studies on a New Phosphonate Carbanion

A new dimethyl 2,7-dichloro-9-fluorenyl phosphonate carbanion (2) has been generated and reacted with a series of aromatic aldehydes to give 9-arylidene-2,7-dichlorofluorenes (4a-r) in good yields.The reaction of 2 with isophthalaldehyde and terephthalaldehyde give 1,3-bis(2,7-dichloro-9-fluorenylidene)xylene (4t), respectively.The structural assignments of the phosphonate (1) and the resulting products are based on spectral data.The phosphonate shows a good antibacterial activity in soil.

Isolation & Reaction of a New Arsonium Ylid: 2,7-Dichlorofluorenylidenetriphenylarsenane

A new stabilized arsonium ylid, 2,7-dichlorofluorenylidenetriphenylarsenane (2) has been reacted with a variety of substituted benzaldehydes to give 2,7-dichloro-9-arylidenefluorenes.Similarly, the ylid (2) also couples with furfural and cinnamaldehyde to give 2,7-dichloro-9-furfurylidenefluorene and 2,7-dichloro-9-cinnamylidenefluorene in good yields.Bis-fluorenylidene derivatives are obtained when 2 reacts with isophthalaldehyde or terephthalaldehyde.The products have been characterised by elemental analyses, IR and PMR data.

Studies on Ylids: Isolation and Reactions of a New Stabilized Phosphonium Ylid

(2,7-Dichlorofluorenylidene)triphenylphosphonium ylid (2), a new phosphonium ylid, has been synthesized by the action of ethanolic sodium ethoxide on its precursor (2,7-dichlorofluorenyl)triphenylphosphonium bromide (1).It reacts with a series of substituted benzaldehydes (3a-n) to give 9-substituted-benzylidene-2,7-dichlorofluorenes (4a-n) in 45-80 percent yields.A similar reaction of 2 with furfural and cinnamaldehyde gives 9-furfurylidene-2,7-dichlorofluorene (4o) and 9-cinnamylidene-2,7-dichlorofluorene (4p)in good yields.The reaction of 2 with isophthaldehyde and terephthaldehyde gives 9(m-formylbenzylidene)-2,7-dichlorofluorene (4q) and 9-(p-formylbenzylidene)-2,7-dichlorofluorene (4r) or 2,2',7,7'-tetrachloro-isophthalal-9,9-difluorene and 2,2',7,7'-tetrachloro-terephthal-9,9'-difluorene respectively depending upon the reaction conditions.