555-89-5

Usage

InChI:InChI=1/C13H10Cl2O2/c14-10-1-5-12(6-2-10)16-9-17-13-7-3-11(15)4-8-13/h1-8H,9H2

Upstream product

• 75-09-2 dichloromethane 
• 1193-00-6 sodium 4-chlorophenolate 
• 75-11-6 diiodomethane 
• 106-48-9 4-chloro-phenol 
• 1121-74-0 potassium 4-chlorophenoxide 
• 288-32-4 1H-imidazole 
• 21151-56-4 p-chlorophenoxymethyl chloride 

Downstream Products

• 34265-75-3 Bis-(4-Chlor-Phenoxy)-Methylchlorid 
• 121077-71-2 Dichlorobis(4-chlorophenoxy)methane 

Relevant academic research and scientific papers

Room-temperature ionic liquid-promoted Williamson's synthesis of ethers: A facile synthesis of diaryloxymethanes

A simple and efficient method has been developed for the synthesis of phenolic ethers using room-temperature ionic liquid, not only as solvent but also as promoter. Ionic liquid was recycled and subsequently reused without any loss of the product. Copyright Taylor & Francis, Inc.

Practical synthesis of diaryloxymethanes

Diaryloxymethanes were prepared by treating phenols with sodium hydride and dichloromethane in N-methyl-pyrrolidinone (NMP) at 40°C.

Practical synthesis of diaryloxymethanes

Diaryloxymethanes were prepared by treating phenols with sodium hydride and dichloromethane in N-methyl-pyrrolidinone (NMP) at 40°C.

One step synthesis of imidazole and benzimidazole acycloaromatic nucleoside analogs

A facile and rapid method for the synthesis of novel imidazole and benzimidazole aromatic acyclic nucleosides is described. Synchronous N-alkylation of imidazole or benzimidazole and potassium aryloxide with methylene iodide in the presence of triethylami

Synthesis of Diaryloxymethanes using Poly(ethylene glycol) as a Phase-transfer Catalyst

Diaryloxymethanes have been synthesized in high yields under conditions of solid-liquid phase-transfer catalysis using poly(ethylene glycol)-600 (PEG-600) as the catalyst.

Catalytic Ability of Octopus-Type Calixarene in the Formation of Ethers from Phenols and Alkyl Halides or 1-Chloro-4-nitrobenzene

The formation of ethers was catalyzed by 5,11,17,23,29,35-hexa-p-t-butyl-37,38,39,40,41,42-hexakis(3,6,9-trioxadecyloxy)calixarene (1).It was found that the calixarene-catalyzed reaction of phenol with benzyl bromide in the presence of KOH in CH2Cl2 yields only the O-alkylated product and this reaction proceeds according to Michaelis-Menten type kinetics.The calixarene 1 also catalyzed the reactions of phenols with dichloromethane and 1-chloro-4-nitrobenzene.

POLYMER SUPPORTED REAGENTS: AN EFFICIENT METHOD FOR THE SYNTHESIS OF DIARYLOXYMETHANES

Diaryloxymethanes were synthesized in high yield and in high purity by the treatment of polymer supported phenoxide ions with dichloromethane.

Catalytic Activity of an Octopus-type Calixarene on the Formation of Ethers

5,11,17,23,29,35-Hexa-p-tert-butyl-37,38,39,40,41,42-hexakis-(3,6,9-trioxadecyloxy)calixarene catalyzes the formation of an ether and bisphenoxymethanes through the Williamson synthesis.

Kinetics of Reaction between Methylene Iodide and Phenoxide Ion

The kinetics of reaction between methylene iodide and phenoxide ion have been studied in 50 percent (v/v) aq.DMSO, aq.DMF and aq. acetone.The activation parameters for the reaction have been determined in aq.DMSO.The reactivity pattern has been rationalized in the light of Hammett's linear free energy relationship.The reaction essentially involves attack on the oxygen atom of phenoxide ion.The validity of the isokinetic relationship has been examined using Exner's method.

Alkyl 4-[o-(substituted methyleneamino)-phenyl]-3-thioallophanate miticides and fungicides

Various alkyl 4-[o-(substituted methyleneamino)phenyl]3-thioallophanates are useful as fungicides and mite ovicides. The compounds are prepared by reacting alkyl 4-(o-aminophenyl)-3-thioallophanates with aldehydes or trialkyl orthoformates. Some of the compounds are prepared by further reacting the reaction product of an alkyl 4-(o-aminophenyl)-3-thioallophanate and a trialkyl orthoformate with a primary or secondary amine. Exemplary species are methyl 4-[o-(o-fluorobenzylideneamino)phenyl]-3-thioallophanate, methyl 4-[o-(4-methylbenzylideneamino)phenyl]-3-thioallophanate and methyl 4-[o-(2-furfurylideneamino)phenyl]-3-thioallophanate.