THE REACTION OF CYANOGEN BROMIDE WITH THE SODIUM SALTS OF CARBOXYLIC ACIDS: I. THE REACTION OF CYANOGEN BROMIDE WITH SODIUM BENZOATE

1953 ◽  
Vol 31 (11) ◽  
pp. 1127-1130 ◽  
Author(s):  
D. E. Douglas ◽  
Jean Eccles ◽  
Anne E. Almond

The main products of the reaction of cyanogen bromide with sodium benzoate at 250 ° to 300 °C. are carbon dioxide, benzonitrile, and sodium bromide. Tracer studies have shown that the carbon of the carbon dioxide is derived almost entirely from the cyanogen bromide.

1958 ◽  
Vol 36 (9) ◽  
pp. 1256-1259 ◽  
Author(s):  
D. E. Douglas ◽  
Anna Mary Burditt

Cyanogen bromide reacts with the sodium salts of lower aliphatic acids at 250-300 °C to form an α-keto isocyanate as the primary product. The latter undergoes subsequent pyrolytic decomposition to a nitrile and carbon dioxide. A mechanism is proposed to account for the observed interchange of labelled carbon atoms between the CN group of the cyanogen bromide and the carboxyl group of the salt in the over-all reaction.


1972 ◽  
Vol 27 (5) ◽  
pp. 528-530 ◽  
Author(s):  
Helga Wittmann ◽  
Helmut Rathmayr

Benzylmalonyl Chloride reacts in the presence of sodium acetate in boiling benzene to give tribenzyl-phloroglucinol-triacetate, however with sodium chloroacetate to 3,5-dibenzyl-6-phenethylpyran-2,4-dion. In both cases trimerisation of benzylketene or benzylketene carboxylic acid chloride occurs. On the other hand, benzylmalonylchloride reacts with sodium benzoate and sodium phenylacetate via a dimeric benzylketene carboxylic acid chloride under the loss of phosgene to yield cyclopentadienyl derivatives.


1933 ◽  
Vol 25 (10) ◽  
pp. 1174-1176 ◽  
Author(s):  
Agnes Fay Morgan ◽  
Catharine I. Langston ◽  
Anna Field

Author(s):  
Weixing Li ◽  
Sonia Melandri ◽  
Luca Evangelisti ◽  
Camilla Calabrese ◽  
Annalisa Vigorito ◽  
...  

The interaction between carbon dioxide and planar carboxylic acids has been investigated through the analysis of the microwave spectrum of the acrylic acid·CO2 complex and quantum chemical modeling of the...


1959 ◽  
Vol 37 (7) ◽  
pp. 1127-1131 ◽  
Author(s):  
H. Heusinger ◽  
R. J. Woods ◽  
J. W. T. Spinks

Bromal labelled with C14 in the carbonyl group has been used to show that small amounts of carbon dioxide and carboxylic acids are produced in the radiolysis of aqueous bromal solutions. G values for the production of CO2 and carboxylic acid are about 7.5% and 15% of those for HBr production, respectively. The observed yield of carboxylic acid is in agreement with that found by titration.


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