Technical documentation

Non-rearrangement Reactions of the Neopentyl-Oxygen Bond. New Syntheses of Neopentyl Halides

By: 
Leo H. Sommer
Herbert D. Blankman
Paul C. Miller

New syntheses for neopentyl bromide and neopentyl chloride are reported which make these interesting aliphatic halides readily available in contraste to the previous methods used. These syntheses also provide unequivocal examples of reactions of the neopentyl-oxygen bond proceeding without rearrangement.

Synthesis and X-ray structural study of 1-adamantylmethyl 2-cyanoacrylate and 1,10-decanediol bis-2-cyanoacrylate

By: 
V. N. Khrustalev
O. V. Shishkin
S. V. Lindeman
Yu. T. Struchkov
M. A. Galkina
Yu. G. Gololobov

I-Adamantylmethyl 2-cyanoacrylate (1) was prepared by the reaction of 2-cyanoacryloyl chloride with 1-adamantylmethanol . 1,10-Decanediol bis-2-cyanoacrylate (2) was synthesized by transesterification of methyl 2-cyanoacrylate with 1,10-decanediol. Esters1 and2 were studied by X-ray structural analysis.

Novel alpha-cyanoacrylate and adhesive composition.

By: 
Hiroyuki Mikuni
Toshiyuki Chikusa

A novel neopentyl alpha -cyanoacrylate is provided. It has superior adhesive properties even at high temperatures and whitening-preventing property.

Solid Cyanoacrylate Adhesive Composition and Method for its Use

US6797107
By: 
Dimiter L. Kotzey

A solid cyanoacrylate adhesive composition is disclosed which can be applied to a substrate in solid form and which polymerizes into an adhesive polymer upon liquefying. Preferably the solid cyanoacrylate composition liquefies at temperatures slightly above room temperature and polymerizes upon liquification. -caprolactones are used as a solidifying polymer with cyanoacrylate monomers and other additives to form the solid cyanoacrylate adhesive composition.

Cyanoacrylate Esters

GB1048906
By: 
Benjamin David Halpern
Jack Dickstein
Rose-Marie Hoegerle

The invention comprises compounds of the formula <1048906><1048906><1048906><1048906><1048906><1048906><1048906>

Practical Syntheses of Neopentyl Alcohol and sec-Butyl Ethyl Ether Using Marukasol as a Solvent

By: 
Yoshifumi Yuasa
Yasushi Kato

The Sealing Properties of Methyl 2-Cyanoacrylate as an Adhesive in Dentistry

By: 
Mohamed AF Know.Assah
Ernest A. Sahs

LE PROPRIETATES IMPERMEABILISATORI DE 2-CYANOACRYLATO METHYLIC USATE COMO AGENTE ADHESIVE IN LE DENTISTERIA.—Le proprietates impermeabilisatori de adhesive 2-cyanoacrylato methylic esseva comparate con illos de varie materiales de cementation que es currentemente usate in le dentisteria. 2-cyanoacrylato methylic, cemento a phosphato de zinc, cemento a oxydo de zinc e eugenol, e cemento Grip esseva usate in cementar applicatos plastic a platte superficies de 36 extrahite dentes human.

Process for the Manufacture of Methyl Cyanoacrylate

US5455369
By: 
Eric A. Meier
Dilip K. Ray-Chaudhuri
Jules E. Schoenberg

A process for preparing methyl .alpha.-cyanoacrylate in which methyl cyanoacetate is reacted with formaldehyde to form a polymer, which is subsequently depolymerized to the monomeric product, comprises using an ester of poly(ethylene glycol) as the solvent for the polymerization and depolymerization reactions.

Process for the manufacture of methyl cyanoacrylate

EP0714887
By: 
Eric A. Meier
Dilip K. Ray-Chaudhuri
Jules E. Schoenberg

Prepn. of methyl alpha-cyanoacrylate comprises reacting methyl cyanoacetate with HCHO in a solvent of a poly(ethylene glycol)di-acetate, dipropionate, or dibutyrate, having a number average molecular wt. of 200-400. The formed polymer is then depolymerised to the monomeric prod. the purity of yield is 96% or better.

 

Synthesis and degradation of poly (alkyl α-cyanoacrylates)

In order to study structure-tissue reactivity relationships and ultimately develop a less necrotizing adhesive, this laboratory undertook a study of the synthesis and degradation of the homologous series of α-cyanoacrylate monomers and polymers. A method for synthesizing high purity cyanoacrylates and some of their chemical and physical properties and presented. In vitro kinetics studies under heterotgeneous and homogeneous conditions indicate that cyanoacrylate polymers degrade by hydrolytic scission of the polymer chain.

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