Reversibility of the ring-opening step in the acid hydrolysis of cyclic acetophenone acetals

1993 ◽  
pp. 1723 ◽  
Author(s):  
Robert A. McClelland ◽  
Brian Watada ◽  
Calvin S. Q. Lew
Keyword(s):  
Acid Hydrolysis ◽  
Ring Opening ◽  
Hydrolysis Of

ChemInform Abstract: Reversibility of the Ring-Opening Step in the Acid Hydrolysis of Cyclic Acetophenone Acetals (I).

ChemInform ◽  
2010 ◽  
Vol 25 (3) ◽  
pp. no-no
Author(s):  
R. A. MCCLELLAND ◽  
B. WATADA ◽  
C. S. Q. LEW
Keyword(s):  
Acid Hydrolysis ◽  
Ring Opening ◽  
Hydrolysis Of

Ring Opening of Dihydro-1,4-oxathiins

1973 ◽  
Vol 51 (16) ◽  
pp. 2650-2658 ◽  
Author(s):  
Maurice Armand Corbeil ◽  
Michael Curcumelli-Rodostamo ◽  
Robert James Fanning ◽  
Bruce Allan Graham ◽  
Marshall Kulka ◽  
...  
Keyword(s):  
Carboxylic Acid ◽  
Acid Hydrolysis ◽  
Ring Opening ◽  
Acid Hydrazide ◽  
Ring Cleavage ◽  
Carboxylic Acid Hydrazide ◽  
Carbonyl Chloride ◽  
Hydrolysis Of

Acid hydrolysis of 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxanilide gives 2-(2-hydroxyethylthio)-acetoacetanilide enol. 3-Carbonyl-substituted 5,6-dihydro-1,4-oxathiins were found to undergo ring cleavage by nucleophilic nitrogen attack on C-2. Thus the following reactions were observed: 3-acetyl-5,6-dihydro-2-methyl-1,4-oxathiin on treatment with hydrazine gives 4-(2-hydroxyethylthio)-3,5-di-methylpyrazole, instead of the hydrazone. The 1,4-oxathiins, N-(5,6-dihydro-2-methyl-1,4-oxathiin-3-ylcarbonyl)-N′-phenylurea and 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxylic acid hydrazide rearrange to give 5-(2-hydroxyethylthio)-6-methyl-1-phenyluracil and 4-(2-hydroxyethylthio)-3-methyl-2-pyrazolin-5-one, respectively. Finally, treatment of 5,6-dihydro-2-methyl-1,4-oxathiin-3-carbonyl chloride with 2-aminopyridine and with 2-aminopyrimidine affords 4H-3-(2-hydroxyethylthio)-2-methyl-pyrido[1,2-a]pyrimidin-4-one and 4H-3-(2-hydroxyethylthio)-2-methylpyrimido[1,2-a]pyrimidin-4-one, respectively, as the predominant products.

DETERMINATION OF MICRO-AMOUNTS OF 5β-PREGNAN-3α-OL-20-ONE IN URINE USING INFRARED-SPECTROMETRY

1962 ◽  
Vol 41 (2) ◽  
pp. 234-246 ◽  
Author(s):  
H. J. van der Molen
Keyword(s):  
Infrared Spectrum ◽  
Quantitative Determination ◽  
Acid Hydrolysis ◽  
Chromatographic Separation ◽  
Pure Form ◽  
Infrared Spectrometry ◽  
Hydrolysis Of

ABSTRACT A procedure for the quantitative determination of 5β-pregnan-3α-ol-20-one in urine is described. After acid hydrolysis of the pregnanolone-conjugates in urine, the free steroids are extracted with toluene. Pregnanolone is isolated in a pure form as its acetate; after chromatographic separation of the free steroids on alumina, the fraction containing pregnanolone is acetylated and rechromatographed on alumina. Quantitative determination of the isolated pregnanolone-acetate is carried out with the aid of the infrared spectrum recorded by a micro KBr-wafermethod. The reliability of the method under various conditions is discussed under the headings, specificity, accuracy, precision and sensitivity. It is possible to determine 30–40 μg pregnanolone in a 24-hours urine portion with a precision of 25%.

Optimization of technological modes of cold acid hydrolysis of potato starch

2020 ◽  
Vol 26 (3) ◽  
pp. 222-233
Author(s):  
M. Alekseenko ◽  
V. Litvyak ◽  
A. Sysa ◽  
E. Hrabovska ◽  
O. Galenko
Keyword(s):  
Acid Hydrolysis ◽  
Potato Starch ◽  
Hydrolysis Of

FLOWTHROUGH ACID HYDROLYSIS OF RAPESEED STALKS

2012 ◽  
Vol 11 (12) ◽  
pp. 2313-2318
Author(s):  
Theodor Malutan ◽  
Adina Elena Panzariu
Keyword(s):  
Acid Hydrolysis ◽  
Hydrolysis Of

scholarly journals Tagasaste, leucaena and paulownia: three industrial crops for energy and hemicelluloses production

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Alberto Palma ◽  
Javier Mauricio Loaiza ◽  
Manuel J. Díaz ◽  
Juan Carlos García ◽  
Inmaculada Giráldez ◽  
...  
Keyword(s):  
Activation Energy ◽  
Acid Hydrolysis ◽  
Energy Production ◽  
Combustion Process ◽  
Operating Conditions ◽  
Raw Material ◽  
Energy Of Combustion ◽  
Increasing Temperature ◽  
Hydrolysis Of ◽  
Chamaecytisus Proliferus

Abstract Background Burning fast-growing trees for energy production can be an effective alternative to coal combustion. Thus, lignocellulosic material, which can be used to obtain chemicals with a high added value, is highly abundant, easily renewed and usually inexpensive. In this work, hemicellulose extraction by acid hydrolysis of plant biomass from three different crops (Chamaecytisus proliferus, Leucaena diversifolia and Paulownia trihybrid) was modelled and the resulting solid residues were used for energy production. Results The influence of the nature of the lignocellulosic raw material and the operating conditions used to extract the hemicellulose fraction on the heat capacity and activation energy of the subsequent combustion process was examined. The heat power and the activation energy of the combustion process were found to depend markedly on the hemicellulose content of the raw material. Thus, a low content in hemicelluloses resulted in a lower increased energy yield after acid hydrolysis stage. The process was also influenced by the operating conditions of the acid hydrolysis treatment, which increased the gross calorific value (GCV) of the solid residue by 0.6–9.7% relative to the starting material. In addition, the activation energy of combustion of the acid hydrolysis residues from Chamaecytisus proliferus (Tagasaste) and Paulownia trihybrid (Paulownia) was considerably lower than that for the starting materials, the difference increasing with increasing degree of conversion as well as with increasing temperature and acid concentration in the acid hydrolysis. The activation energy of combustion of the solid residues from acid hydrolysis of tagasaste and paulownia decreased markedly with increasing degree of conversion, and also with increasing temperature and acid concentration in the acid hydrolysis treatment. No similar trend was observed in Leucaena diversifolia (Leucaena) owing to its low content in hemicelluloses. Conclusions Acid hydrolysis of tagasaste, leucaena and paulownia provided a valorizable liquor containing a large amount of hemicelluloses and a solid residue with an increased heat power amenable to efficient valorization by combustion. There are many potential applications of the hemicelluloses-rich and lignin-rich fraction, for example as multi-components of bio-based feedstocks for 3D printing, for energy and other value-added chemicals.

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