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Carbonylation chloride

Methyl a-D-mannopyranoside was treated in succession with p-toluene-sulfonyl chloride, carbonyl chloride, and benzoyl chloride, and, without isolating the intermediates, there was obtained in 37% yield methyl 4-0-l enzoyl-2,3-O-carbony 1-6-0-(p-tolylsulfonyl ) -D-mannoside. The tos-yloxyl group of the latter was replaced by iodine, and hydrogenation of the 6-iodo derivative in the presence of a nickel boride catalyst gave methyl 4-0-benzoyl-2,3-0-carbonyl-6-deoxy- -D-mannoside. Treatment of the latter with hydrogen bromide in acetic acid gave crystalline 4-0-benzoyl-2,3-0-carbonyl-6-deoxy-a-D-mannosyl bromide (8) (16). The... [Pg.18]

Conversion of Acid Halides into Acids Hydrolysis Acid chlorides react with water to yield carboxylic acids. This hydrolysis reaction is a typical nucleophilic acyl substitution process and is initiated by attack of water on the acid chloride carbonyl group. The tetrahedral intermediate undergoes elimination of Cl and loss of H+ fo give the product carboxylic acid plus HC1. [Pg.802]

MRH Bromine 1.21/91, carbon tetrachloride 2.89/83, chlorine 3.85/82 Silane burns in contact with bromine, chlorine or covalent chlorides (carbonyl chloride, antimony pentachloride, tin(IV) chloride, etc.) [1], Extreme caution is necessary when handling silane in systems with halogenated compounds, as a trace of free halogen may cause violent explosions [2],... [Pg.1688]

Carhonyl chloride, Carbonic dichloride, Chloroformyl chloride Carbonyl chloride, Carbon oxychloride Carbonyl chloride, Carbonic dichloride, Chloroformyl chloride Carbonyl chloride. Carbon oxychloride... [Pg.33]

Without isolation of the intermediates, methyl a-D-mannopyranoside (38) was treated in succession with p-toluenesulfonyl chloride, carbonyl chloride, and benzoyl chloride, giving methyl 4-0-benzoyl-2,3-0-carbonyl-... [Pg.295]

Corbonic Acid, H2C03. The soln of C02 in H O exhibits feeble acid props it is unstable, however, and has never been isolated it is known only in the form of its salts (carbonates), acid salts 0bicarbonates), amides (carbamic acid or urea), and as acid chlorides (carbonyl chloride). This is also an old term for carboxylic acid Ref Hackh s(1944), 169... [Pg.456]

Of all these processes only flame hydrolysis is used to produce oxides with high surface areas on a large industrial scale Therefore, the emphasis of this article lies on this subject In general, this process is suitable for any volatile compound that can be decomposed at a high temperature to form an oxide Possible precursor compounds that can be used are metal chlorides carbonyls such as Ni(CO)4 or Fe(CO)s, and volatile alcoholates Reactions that have been studied are, for example, the manufacture of AUOj from A1CU [3]... [Pg.56]

Dudis, D. S., Everhart, J. B, Branch, T. M., and Hunnicutt, S. S., Hydrogen bond energies of hydrogen chloride-carbonyl complexes, J. Phys. Chem. 100, 2083-2088 (1996). [Pg.132]

Acid chloride—olefin addition and Friedel-Crafts cyclization A previous procedure was improved by use of methylene chloride as solvent rather than carbon disulfide. To check the progress of the reaction, one can quench a 2 3-ml. aliquot with water in a test tube, separate and dry the organic phase, and evaporate. The infrared spectrum will show disappearance of the acid chloride carbonyl band at 5.6(1 /j and appearance of the... [Pg.11]

AMINO GROUP Boron trifluoride ether-ale. l-r-Bulyloxycarbonyltriazole-1,2,4, Di-t-butyl dicarbonate. 4-Dimethylamino-1-t-butyloxycarbonyl pyridinium chloride. CARBONYL GROUP Ceric ammonium nitrate. 1,2-Dihydroxy-3-bromopropane. Sodium N-chloro-p-toluenesulfonamide. Thallium(lll) nitrate. Trichloroethanol. Trimcthylsilyl cyanide. Chloromethyl methyl sulfide. N,N -Diisopropylhydra-zinc. Trichloroethanol. [Pg.587]

In the presence of titanium(IV) chloride or aluminum chloride, carbonyl compounds such as aldehydes, ketones, acetals, and acid halides are allylated with allylic silanes (eq (12)) [9]. The conjugate addition to enones is also reported (eq (13)) [10],... [Pg.395]

Cobalt and Ni catalyze the carbonyiation of strained cyclic esters such as /3-propiolactone and butyrolactone . Palladium chloride carbonylates esters of allyl alcohol to 3-butenoic anhydrides at 100° and 9.6 MPa. ... [Pg.541]

Benzyl chloride, carbonylation, phase transfer catalysis, phenyl acetic acid 1. INTRODUCTION... [Pg.875]

Carbonyl chloride Carbonyl fiuoride Chloroacetyl chloride Chloroacetylene... [Pg.1404]

SYNONYMS carbon oxychloride, carbonyl chloride, carbonyl dichloride, chloroformyl chloride, disphosgene. [Pg.838]

Synonyms/Trade Names Carbon oxychloride, Carbonyl chloride. Carbonyl dichloride, Chloroformyl chloride ... [Pg.253]


See other pages where Carbonylation chloride is mentioned: [Pg.14]    [Pg.540]    [Pg.139]    [Pg.325]    [Pg.937]    [Pg.526]    [Pg.57]    [Pg.111]    [Pg.859]    [Pg.879]    [Pg.424]    [Pg.203]    [Pg.63]    [Pg.457]    [Pg.112]    [Pg.493]    [Pg.859]    [Pg.969]   
See also in sourсe #XX -- [ Pg.187 , Pg.362 ]




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Acyl chlorides, catalyzed carbonylation

Acyl chlorides, catalyzed carbonylation ketones

Acylation by carbonyl chlorides

Alcohols carbonyl chloride fluoride

Aldehydes carbonyl chloride fluoride

Aldehydes from carbonyl chlorides

Alkalis carbonyl chloride fluoride

Allyl chloride, carbonylation

Allylic chlorides, carbonylation

Amides acyl chloride carbonylation

Amines carbonyl chloride fluoride

Anthracene-9-carbonyl chloride

Aromatic chlorides, carbonylation

Benzyl chloride, biphasic carbonylation

Benzyl chloride, carbonylation

Bromine carbonyl chloride

CARBONYL ADDITIONS, CERIUM CHLORIDE-PROMOTED

Carbon carbonyl chloride

Carbonyl bromide chloride

Carbonyl bromide chloride decomposition

Carbonyl bromide chloride from phosgene

Carbonyl bromide chloride hydrolysis

Carbonyl bromide chloride metals

Carbonyl bromide chloride organic reactions

Carbonyl bromide chloride reaction with

Carbonyl bromide chloride synthesis

Carbonyl chlorid

Carbonyl chlorid

Carbonyl chloride

Carbonyl chloride

Carbonyl chloride 1168 nomenclature

Carbonyl chloride fluoride

Carbonyl chloride fluoride availability

Carbonyl chloride fluoride determination

Carbonyl chloride iodide

Carbonyl chloride iodide synthesis

Carbonyl chloride ions

Carbonyl chloride ions decomposition

Carbonyl chloride isocyanate

Carbonyl chloride isocyanate synthesis

Carbonyl chloride s. Phosgene

Carbonyl chloride, COCL

Carbonyl chloride, reaction

Carbonyl compounds Acyl chlorides Aldehydes

Carbonyl compounds acid chlorides, reduction

Carbonyl compounds amide chlorides

Carbonyl compounds palladium chloride catalysts

Carbonyl group anhydrides Acyl chlorides

Carbonylation and Reactions of Acyl Chlorides

Carbonylation of allyl chloride

Carbonylation of allylic chlorides

Carbonylation of benzyl chloride

Carbonylations alcohols, palladium chloride

Carbonylations alkenes, palladium chloride

Carbonylations palladium chloride

Carboxylic acids acyl chloride carbonylation

Chloride carbonyl compounds

Chromone-2-carbonyl chlorides

Chromone-2-carbonyl chlorides reactions

Chromone-2-carbonyl chlorides synthesis

Copper carbonyl chloride

Copper carbonyl chloride, [CuCl

Copper chloride carbonyl compounds

Direct carbonylative coupling, palladium chloride

Esters acyl chloride carbonylation

Fluorine carbonyl chloride

Fluoroformates from carbonyl chloride fluoride

From carbonyl chloride fluoride

Hydrolysis carbonyl chloride fluoride

Metal carbonyls chloride catalysis

Methyl chloride carbonylation

Organic compounds carbonyl bromide chloride

Oxadiazole carbonyl chloride

Oxalyl Chloride reactions with carbonyl groups

Oxidative carbonylations palladium®) chloride

Palladium carbonyl chloride

Palladium chloride carbonyl compounds

Phosgene, or Carbonyl Chloride

Quinoline-3-carbonyl chloride, 2-phenylFriedel-Crafts reaction

Reaction with carbonyl chloride fluoride

Reactivity carbonyl chloride fluoride

Rhodium carbonyl chloride

Rubber carbonyl chloride fluoride

Ruthenium complexes carbonyl chlorides

Standard Carbonyl chloride

Suffix carbonyl chloride

Terminal oxidative carbonylations, palladium®) chloride

Thioureas, reaction with carbonyl chloride

Toxicity carbonyl chloride fluoride

Unsaturated carbonyl compounds) From acyl chlorides

Unsaturated carbonyl compounds) chloride

Ureas, reaction with carbonyl chloride

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