Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Amine From alcohol

Carbon oxide sulfide Alcohols from amines... [Pg.366]

From what you know about wetting, contact angles, and spread monolayers, explain why a Langmuir-Blodgett layer will deposit as a F type if there are nonpolar fatty acids, yet will switch to a Z-type deposition if bipolar alcohols or amines are added (see Refs. 175, 176). What defines the critical contact angle for the deposition change ... [Pg.563]

The rather unreactive chlorine of vinyl chloride can be displaced with nucleophiles by the catalytic action of PdCb. The conversion of vinyl chloride to vinyl acetate (797) has been studied extensively from an industrial standpoint[665 671]. DMF is a good solvent. 1,2-Diacetoxyethylene (798) is obtained from dichloroethylene[672]. The exchange reaction suffers steric hindrance. The alkenyl chloride 799 is displaced with an acetoxy group whereas 800 and 801 cannot be displaccd[673,674]. Similarly, exchange reactions of vinyl chloride with alcohols and amines have been carried out[668]. [Pg.246]

At the other end of the reaction, deviations from idealized rate laws are attributed to secondary reactions such as degradations of acids, alcohols, and amines through decarboxylation, dehydration, and deamination, respectively. The step-growth polymers which have been most widely studied are simple... [Pg.287]

Potassium Bases. Potassium metal is used to prepare potassium bases from reactions of the metal with alcohols and amines. [Pg.519]

Dicyanoacetylene, 2-hiitynedinitri1e, is obtained from dimethyl acetylenedicarboxylate by ammonolysis to the diamide, which is dehydrated with phosphoms pentoxide (44). It bums in oxygen to give a flame with a temperature of 5260 K, the hottest flame temperature known (45). Alcohols and amines add readily to its acetylenic bond (46). It is a powerhil dienophile in the Diels-Alder reaction it adds to many dienes at room temperature, and at 180°C actually adds 1,4- to benzene to give the bicyclo adduct (7) [18341 -68-9] C QHgN2 (47). [Pg.405]

PdCl2(Ph3P)2, dimedone, THF, 95% yield. This method is also effective for removing the allyloxycarbonyl group from alcohols and amines. [Pg.248]

Chirazymes. These are commercially available enzymes e.g. lipases, esterases, that can be used for the preparation of a variety of optically active carboxylic acids, alcohols and amines. They can cause regio and stereospecific hydrolysis and do not require cofactors. Some can be used also for esterification or transesterification in neat organic solvents. The proteases, amidases and oxidases are obtained from bacteria or fungi, whereas esterases are from pig liver and thermophilic bacteria. For preparative work the enzymes are covalently bound to a carrier and do not therefore contaminate the reaction products. Chirazymes are available form Roche Molecular Biochemicals and are used without further purification. [Pg.520]

Aryl esters, prepared from the phenol and an acid chloride or anhydride in the presence of base, are readily cleaved by saponification. In general, they are more readily cleaved than the related esters of alcohols, thus allowing selective removal of phenolic esters. 9-Fluorenecarboxylates and 9-xanthenecarboxylates are also cleaved by photolysis. To permit selective removal, a number of carbonate esters have been investigated aryl benzyl carbonates can be cleaved by hydrogenolysis aryl 2,2,2-trichloroethyl carbonates by Zn/THF-H20. Esters of electron-deficient phenols are good acylating agents for alcohols and amines. [Pg.276]

In the presence of DCC, 140 is allowed to react with both l-hydroxy-5-nitroindole (36) and 1-hydroxy-1,2,3-benzotriazole (141). Interestingly, their corresponding active esters, 142 and 143, are obtained in excellent yields as stable crystalline compounds. Both compounds are found to react with variety of nucleophiles, such as alcohols and amines, to produce 144 and 145 in good to excellent yields, as can be seen from the typical examples shown in Scheme 22 (2001H2361). As aresult, it becomes possible to produce various kinds of derivatives of wasabi phytoalexin utilizing 142 and 143. [Pg.122]

The Frumkin isotherm can be regarded as a general isotherm from which both the Temkin and Langmuir isotherms can be obtained as special cases. Szklarska-Smialowski and Wieczorek found that the adsorption of various aliphatic compounds (acids, alcohols and amines) on steel in H2SO4 conformed with the Frumkin isotherm. [Pg.1189]

Acid chloride, alcohols from, 804 alcoholysis of, 802-803 amides from, 803-804 amines from, 933-935 amjnolysis of, 803-804 carboxylic acids from, 802 electrostatic potential map of, 791... [Pg.1281]

Neopentyl alcohol, 40, 76 Nickel catalyst for hydrogenation of resorcinol, 41, 56, 57 Nitramines from amines and acetone cyanohydrin nitrate, 43, 84 Nitration, of amines to nitramines by acetone cyanohydrin nitrate, 43, 83... [Pg.118]


See other pages where Amine From alcohol is mentioned: [Pg.494]    [Pg.547]    [Pg.102]    [Pg.83]    [Pg.358]    [Pg.9]    [Pg.115]    [Pg.495]    [Pg.494]    [Pg.547]    [Pg.102]    [Pg.83]    [Pg.358]    [Pg.9]    [Pg.115]    [Pg.495]    [Pg.28]    [Pg.139]    [Pg.227]    [Pg.111]    [Pg.498]    [Pg.103]    [Pg.403]    [Pg.208]    [Pg.238]    [Pg.299]    [Pg.65]    [Pg.67]    [Pg.277]    [Pg.238]    [Pg.1069]    [Pg.1283]    [Pg.1284]    [Pg.1290]    [Pg.1302]    [Pg.101]    [Pg.439]   
See also in sourсe #XX -- [ Pg.494 , Pg.1398 , Pg.1643 ]

See also in sourсe #XX -- [ Pg.8 ]




SEARCH



Acid chloride, alcohols from reaction with amines

Alcohols amination

Alcohols amines

Allylically Transposed Amines from Allylic Alcohols 3,7-Dimethyl

Amides from alcohols and amines

Amine From allylic alcohol

Amines from tertiary alcohols, table

Amino-alcohols from amines

Cyclic Amines from Amino Alcohols or Diols

From aminals

From amines

Hydroxy amines from halo alcohols

Lithium aluminum hydride reduction, alcohols amines from

Process, continuous amines from alcohols

Synthesis of Amides from Alcohols and Amines

© 2024 chempedia.info