PREPARATION OF KETENE FROM GLACIAL ACETIC ACID. METHYL ACETATE, AND ETHYL ACETATE

1952 ◽  
Vol 30 (4) ◽  
pp. 332-347 ◽  
Author(s):  
K. K. Georgieff

Laboratory studies were carried out to determine whether methyl and ethyl acetates could be pyrolyzed to give yields and conversions to ketene comparable to those obtainable from acetic acid. Acetic acid was pyrolyzed to ketene and water in the presence of 0.33% triethyl phosphate or phosphoric acid catalyst at 680°–760 °C. and 140–160 mm. Hg absolute. Maximum yield obtained was 80.6% and maximum conversion 34.5%. Methyl acetate was cracked to ketene and methanol at 610°–685 °C. and 95–400 mm. absolute, using triethyl phosphate, phosphoric acid, sulphuric acid, dimethyl sulphate, butyl borate, and silica gelboric acid as catalysts. High yields could be obtained only with phosphates in 2–3% concentration. Maximum yield to ketene, including ketene recovered as acetic acid, was 76% (conversion 31–34%). Maximum yield to methanol was 81.3% (conversion 33–34%). Methyl acetate containing 18% methanol was also cracked but results were poorer. Ethyl acetate, in the presence of 0.33% triethyl phosphate, was pyrolyzed to ketene, ethylene, and water at 630°–685 °C. and 140–190 mm. absolute. Maximum yield of ketene, including ketene recovered as acetic acid, was 85.8%. Maximum conversion to ketene was 35.4% and to ketene plus acetic acid 85.7%. Yields to ethylene were nearly quantitative.

2020 ◽  
Vol 2020 (3) ◽  
pp. 38-43

Amidoalkylating reagents containing a phthalimide group are used in the synthesis of hard-to-reach primary amines and complex heterocyclic compounds. These types of amidoalkylating compounds are suitable reagents for nucleophilic substituted reactions in acidic media due to their resistance to acids. Result of reactions of amidoalkylating reagents-N-hydroxyethylphthalimide and N-hydroxymethylphthalimide with aliphatic carbonic acids can also produce new bactericidal and fungicidal esters. In this study, halogen acids reacted with N-hydroxymethylphthalimide monochloric acetic acid, monobromic acetic acid, monoiodic acetic acid, trifluoric acetic acid and trichloroacetic acid, as well as, N-b-hydroxyethylphthaleidyl monohydric acid. As a result of the reactions, new phthalimidomethyl and phthalimidoethyl esters of haloacetic acids were synthesized. The physical properties of crystalline esters have been determined. The structure of these compounds were confirmed by the analysis of their IR and PMR spectra. The esterification reactions of halogenated acetic acids were carried out in a benzene solvent and a sulfuric acid catalyst with primary alcohols, N-hydroxymethylphthalimide and N-β- beta hydroxyethylphthalimide,. It was found that in a benzene solvent, which increases the rate of bimolecular nucleophilic exchange in primary alcohols, phthalimidoethyl esters of halogen acid are formed in high yields, and phthalimidomethyl esters are formed in low yields. It was shown that the reaction of esterification of halogen acids with N-hydroxymethylphthalimide proceeds with monomolecular nucleophilic exchange.


2000 ◽  
Vol 193 (1) ◽  
pp. 16-28 ◽  
Author(s):  
M.A.Natal Santiago ◽  
M.A. Sánchez-Castillo ◽  
R.D. Cortright ◽  
J.A. Dumesic

Author(s):  
E.A. Edreder ◽  
Mansour Emtir ◽  
Iqbal M Mujtaba

In this study, the (catalysed) esterification process of acetic acid with ethanol producing ethyl acetate and water is modelled using detailed mass and energy balances and thermodynamic properties within gPROMS modelling software (version 3.0.3, 2004). The basic model was taken from Mujtaba and Macchietto (1997) assuming no azeotrope formation in the system. Kinetic (hydrochloric acid as a catalyst at 100 °C) and vapour-liquid equilibrium models are taken from Bogacki et al. (1989) and Suzuki et al. (1970) respectively. Physical properties are calculated using the Ideal Physical Properties Foreign Objective (IPPFO) package interfaced to gPROMS. The performance of the batch reactive distillation is evaluated in terms of the maximum conversion of ethanol to ethyl acetate. Five cases with varying amounts of reactants (including the cases with the reduced amount of water in the feed and keeping the amount of acetic acid and ethanol fixed) are utilized to improve the conversion of ethanol to ethyl acetate. Both piecewise constant and linear reflux ratio profiles (single time interval) are considered as a control variable for the base case while the piecewise constant single reflux ratio strategy is adopted for other optimized cases. The results show that both the maximum conversion and distillate product (base case) are improved using the linear reflux strategy as a control variable compared to those with a constant reflux ratio profile. Increasing the amount of water in the feed leads to a reduction in the conversion and distillate product; moreover, the column was operated at a higher reflux ratio compared to the case without any water in the feed.


2016 ◽  
Vol 1 (4) ◽  
pp. 409-417 ◽  
Author(s):  
Tao Deng ◽  
Yakun Li ◽  
Guofeng Zhao ◽  
Zhiqiang Zhang ◽  
Ye Liu ◽  
...  

We present a microfibrous-structured Nafion–SiO2/SS-fiber solid acid catalyst and demonstrate its separation and reaction efficiency as catalytic distillation (CD) packings for esterification to produce ethyl acetate from acetic acid and ethanol.


2019 ◽  
Vol 14 (9) ◽  
pp. 76
Author(s):  
Duong Quoc Hoan ◽  
Nguyen Thi Hanh ◽  
Truong Minh Luong ◽  
Hoang Thi Nhu Quynh ◽  
Nguyen Hien

A series of Schiff bases were synthesized successfully based on the condensation reaction between 5-nitrovanillin and aromatic amines in moderate and high yields. The condensation underwent better in DCM solvent, acetic acid catalyst and anhydrous MgSO4 as a drying agent and increased the yield up to 100 %.These new Schiff bases were determined with 1H, 13C NMR spectral analysis and compound 3a was studied further HSQC, HMBC, NOSY and MS spectra. The C=N bond exists in E conformation.


2012 ◽  
Vol 550-553 ◽  
pp. 292-295
Author(s):  
Guo Fu Sun ◽  
Jing Li Xu ◽  
Hong Yan Si

Ethyl acetate was synthesized by catalytic distillation using packing solid super acid catalyst of SO42-/Al2O3made by oneself. The effects of process parameters such as the ratio between acetic acid and ethanol, the feed flow rate of ethanol and reflux ratio on catalytic distillation were observed. The best operation parameters were determined. It was beneficial for synthesis of ethyl acetate when n(acetic acid)/n(ethanol) was 1/3, the feed flow rate of ethanol was 3mol/l and reflux ratio was 2.


2020 ◽  
Vol 17 ◽  
Author(s):  
Kalyani K. ◽  
Srinivasa Reddy Kallam

Abstract:: An efficient synthesis of 2-substituted Quinazolin-4(3H)-ones has been developed from isatoic anhydride with various amidoximes by using recyclable polymer supported sulphonic acid catalyst. Excellent functional group compatibil-ity and high yields are the important features of this protocol.


1978 ◽  
Vol 24 (12) ◽  
pp. 2135-2138 ◽  
Author(s):  
K W Jackson

Abstract Each of 65 laboratories analyzed 10 whole-blood samples for erythrocyte protoporphyrin by one or more of several analytical procedures. These procedures were of two types: (a) extraction of protoporphyrin from the erythrocytes into ethyl acetate/acetic acid, re-extraction into hydrochloric acid, and fluorometric measurement; or (b) direct reading in a portable fluorometer (hematofluorometer), with no pretreatment of the blood sample. Interlaboratory correlation was generally poor, especially between laboratories using extraction procedures. Hematofluorometric results intercorrelated better, but they had a low bias as compared to the extraction approach. Nationwide standardization of the test is required to assure satisfactory interlaboratory performance and to identify laboratories whose results are sufficiently accurate to be used for interpretations according to guidelines set forth by the Center for Disease Control for erythrocyte protoporphyrin testing.


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