92594-58-6

Upstream product

• 3395-81-1 4-chlorobenzaldehyde dimethyl acetal 
• 13716-45-5 diethyl trimethylsilyl phosphite 
• 762-04-9 phosphonic acid diethyl ester 
• 122-52-1 triethyl phosphite 

Downstream Products

• 63704-23-4 α,α-diphenylchloroacetophenone 
• 90269-48-0 1-(4-chlorophenyl)-2-methylbutan-1-one 
• 3277-80-3 (4-chlorophenyl)(cyclohexyl)methanone 
• 777038-79-6 1-(4-chlorophenyl)-2-(4-methylphenyl)-propan-1-one 
• 123989-29-7 1-(p-chlorophenyl)-2-cyclopropyl-2-methylethan-1-one 

Relevant academic research and scientific papers

Catalytic synthesis method of alpha-alkoxy p-chlorobenzyl phosphonate

The invention relates to a preparation method of alpha-alkoxy p-chlorobenzyl phosphonate. The alpha-alkoxy p-chlorobenzyl phosphonate is obtained from a compound I and a compound II reacting for 0.1-10 hours at (-20)-50 DEG C under the effect of a catalys

Preparation method of alpha-alkoxy bi-chlorobenzyl phosphonate

The invention relates to a preparation method of alpha-alkoxy bi-chlorobenzyl phosphonate. The alpha-alkoxy bi-chlorobenzyl phosphonate is obtained by performing reaction on a compound I and a compound II at a temperature of minus 20-150 DEG C under the a

Iron-catalyzed cross coupling of P-H/C-O bonds: Efficient synthesis of α-alkoxyphosphorus compounds

An efficient P-C bond-formation through iron-catalyzed cross coupling of P-H/C-O bonds is developed for the first time. This reaction proceeds efficiently to produce the corresponding valuable α-alkoxyphosphorus compounds under mild conditions with a wide generality.

A FACILE SYNTHESIS OF DIETHYL 1-ALKOXY-1-ARYLMETHANEPHOSPHONATES

1-Alkoxy-1arylmethanephosphonates (3) can be prepared by the reaction of arylaldehyde acetal (2) and diethyl trimethylsilylphosphite (1) in the presence of stannic chloride under mild conditions.