4970-23-4

Upstream product

• 64-18-6 formic acid 
• 6326-60-9 diphenyl(2-hydroxyphenyl)methanol 
• 72824-75-0 ((2-methoxyphenyl)methylene)dibenzene 
• 110247-02-4 2-benzhydryl-phenetole 
• 127136-68-9 C₂₃H₂₇N₂O₃P 
• 82392-68-5 1,2,5,6-Dibenzo-3,7-dioxa-4,4,8,8-tetraphenyl-1,5-cyclooctadiene 
• 39777-52-1 1-(2'-bromophenyl)-1,1-diphenylmethane 
• 19672-37-8 3-benzhydryl-pentane-2,4-dione 
• 108-95-2 phenol 
• 119-36-8 methyl salicylate 
• 118-55-8 phenyl Salicylate 
• 91-01-0 1,1-Diphenylmethanol 
• 64-19-7 acetic acid 
• 7647-01-0 hydrogenchloride 

Downstream Products

• 101-81-5 Diphenylmethane 
• 72824-75-0 ((2-methoxyphenyl)methylene)dibenzene 
• 110247-02-4 2-benzhydryl-phenetole 

Relevant academic research and scientific papers

Aspects of the Chemistry of Donor Solvent Coal Dissolution Reactions. The Reduction of Benzophenone and the Diproportionation of Benzhydrol in Hydrocarbon Solvents at High Temperature

The reduction of benzophenone by hydrogen donor molecules such as tetralin and dihydroanthracene to give diphenylmethane was investigated in the temperature range 300-400 deg C.Several lines of evidence indicate that the reaction occurs in three distinct stages.The first stage is a radical process which gives benzhydrol.In the second stage, this intermediate undergoes an SN reaction to produce water and bis(diphenylmethyl) ether.The ether disproportionates in a readily initiated, free radical chain reaction to give diphenylmethane and benzophenone.

Dynamic Induction of Optical Activity in Triarylmethanols and Their Carbocations

A series of artificial triarylmethanols has been synthesized and studied toward the possibility of exhibiting an induced optical activity. The observed chiroptical response of these compounds resulted from the chiral conformation of a triarylmethyl core.

Simple Method for sp2-sp3 and sp3-sp3 Carbon-Carbon Bond Activation in 2-Substituted 1,3-Diketones

Simple and efficient methods were developed for sp2-sp3 and sp3-sp3 C-C bond-activation reactions of 2-substituted 1,3-diketones. 3-Substituted 3-bromopentane-2,4-diones were deacylated in the presence of an aromatic compound and a silica gel supported Bronsted acid containing sulfonic groups. The carbocation formed by cleavage of the sp3-sp3 C-C bond of the dione alkylated the aromatic compound.

INTERMOLECULAR CYCLIZATION OF o-FUCHSONES

o-Fuchsones formed by dehydrohalogenation of o-hydroxyaryl(diaryl)methyl chlorides with tertiary amines undergo a cyclization to eight-membered dimers of the type head to tail.The dimerization reaction is catalyzed by tertiary amines hydrochlorides involving very likely triarylmethyl cation as intermediates.