3. Catalytic application of sulfated tin oxide in organic synthesis 3.1. Synthesis of 7-hydroxy-4-methyl coumarin using Pechmann condensation method Different sulfate content (5 to 30% by weight) containing nanostructure sulfated tin oxides were synthesized from the hydroxylated tin oxide (obtained from precipitation method) and SO42- species of the sulfuric acid. At the temperatures 400, 500, and 600 °C, the so prepared sulfated tin oxide catalysts were calcinated. These catalysts were analyzed in the solvent free synthesis of 7-hydroxy-4-methyl coumarin from ethylacetoacetate:resorcinol (molar ratio 2: 1) at 120 °C by using the Pechmann condensation methodology.49 The FT-IR spectra in pyridine of these catalysts clearly indicated the existance …show more content…
Corma et al also investiagted the effect of the sulfate content and the calcination temperature on the yield of the reaction. One more advantage of the methodology developed is the reusability of the sulfated tin oxide solid acid catalyst. The acidic properties of the sulfated tin oxide catalyst was analyzed by an in situ FT-IR (CO adsorbed …show more content…
The catalyst surface acidity was determined by uisng the TGA/Pyridine sample. The acid strength of the catalyst was analyzed with potentiometric titration with n-butylamine in non-aqueous media. As represented in the Scheme 5, the Friedel-Crafts acylation of toluene was achieved with the prepared sulfated catalysts56 to investigate the catalytic activityA higher yields of the acylation products were obtained with sulfated tin oxide than Al3+-impregnated sulfated zirconia, since STO has greater acidity and higher acid strength. It was also observed that the sulfated tin oxide was found to show maximum higher acidity and higher efficiency for the acylation reaction when sulfate loading was 10 wt%. Among the structural characteristics, acidity and catalytic activity,a good relationship is
3.1 Project Methodology In order to make sure that this project is on track, proper planning and scheduling is crucial. It is necessary to identify the significant key points which are photocatalytic activity of SWCNTs, properties of carbon nanotubes and titanium oxide, available testing procedures using scanning electron microscopy (SEM) and other spectroscopic methods. In this section, a brief detail provided regarding the methods used, sol-gel, hydrothermal and electrospinning. Also, the available tests that will be used are explained.
Introduction SN2 stands for substitution, nucleophilic, bimolecular and occurs in one step where the nucleophile and electrophile react: the nucleophile attacks the electrophile 180° from the leaving group.3 The leaving group is nothing more than a group that leaves the electrophile attacked by the nucleophile. In this experiment the nucleophile is bromide, the electrophile is 1-butanol, and the leaving group is hydroxide. However, bromide must first be obtained from hydrobromic acid which gets bromide from a reaction between sodium bromide and sulfuric acid. The hydrogen and bromide in hydrobromic acid reacts with the oxygen in 1-butanol and the carbon attached to oxygen respectively to form 1-bromobutane. The overall reaction of this procedure
This experiment is performed to test how Daphnia react when exposed to differing levels of copper sulfate so that we may understand what effects it has on underwater organisms. One possible hypothesis is, if the levels of copper sulfate in their environment rise, more of the Daphnia will die because copper sulfate is toxic. Daphnia are members of a collection of small crustaceans that are commonly called water fleas that are commonly found in small lakes and ponds. They reproduce through parthenogenesis, only creating male eggs once food becomes scarce. They eat algae, bacteria, and yeast.
The process of acid-catalyzed hydration of an alkene to and alcohol has valuable properties with practical uses. Naturally, as an alkene, norbornene is not very reactive. It has a strong pi bond, and is also non-polar. However, by hydrating norbornene with the assistance of an acid-catalyst, norborneol is formed. Norborneol, being an alcohol, is much more reactive and has the potential to be further reacted to obtain a certain product.
The reaction to synthesize benzocaine was known as a Fisher esterification reaction. The Fisher esterification was reaction between alcohol and carboxylic acid in the presence of acid. The reaction was used to form an ester. In the experiment, sulfuric acid acted as a catalyst and necessary for this reaction to occur. There was a change between the –OH group of carboxylic acid to an –OCH2CH3 group in the reaction.
Lab Report 5: Acetylsalicylic Acid (Aspirin) Synthesis Name: Divya Mehta Student #: 139006548 Date Conducted: November 19th 2014 Date Submitted: November 26th 2014 Partner’s Name: Kirsten Matthews Lab Section: Wednesday 2:30 L9 IAs Name: Brittany Doerr Procedure: For the procedure, see lab manual (CH110 Lab Manual, Fall 2014) pages 96-98. Wilfrid Laurier University Chemistry Department. Fall 2014. Acetylsalicylic Acid (Aspirin) Synthesis.
Introduction The purpose of this experiment was to learn about Friedel-Crafts alkylations, acylations, and perform the second step in the synthesis of bexarotene. Friedel-Crafts reactions are used to create carbon-carbon bonds to aromatic
Cross Condensation of aldol 2015007632 Dowrie, K Contents Reaction 1 Introduction 1 Experiment Procedure 2 Experimental results 3 Table of calculations 3 Calculations 3 NMR 4 TLC 4 References 5 Reaction Introduction An aldehyde reaction is when aldehydes and keytones, both containing an α-hydrogen in the presence of an alkali group condenses and forms an enone. Acetone has α-hydrogens on each side. The proton can be removed and therefore giving a nucleophile anion. The aldehyde carbonyl is more reactive than the keytone and so it reacts rapidly with the anion.
+ H2O (g) Reaction 4: when a sulphuric acid is added to the solution that contains copper (II) oxide, a double displacement reaction will occur. the copper (II) oxide will react with the sulphuric acid producing copper (II) sulfate and water. The copper and hydrogen gas replace each other. Balanced Chemical Equation: CuO (s) + H2SO4 (aq) —> CuSO4 (aq) + H2O (l) Reaction 5: when zinc is added to the copper (II) sulfate solution, a single displacement reaction will occur.
3.3. Synthetic methodologies for dihydropyrimidinones 3.3.1. Classical method Scheme-1: The conventional method for the synthesis of DHPMs is the one-pot three-component reaction of benzaldehyde, ethyl acetoacetate and urea in the presence of an acid catalyst. The product of this novel one-pot, three components synthesis that precipitated on cooling of the reaction mixture was identified as 3,4-dihydropyrimidin-2(1H)-one and this reaction came to be known as “Biginelli reaction”, or “Biginelli condensation”, or “Biginelli dihydropyrimidine synthesis” after the name of its inventor “Pietro Biginelli”.1 Mechanism Forty years after Biginelli’s initial report, the first mechanism for the synthesis of DHPMs was conducted by Folkers and Johnson
Drapex 6.8, supplied by Galata Chemicals from Louisiana, was the ESO used. Boron trifluoride diethyl etherate, dimethyl benzyl amine, hexanoic anhydride (97%), n-hexanoic acid (99%) and n-octanoic acid (99%) were obtained from Sigma-Aldrich, USA, while sodium chloride and sodium bicarbonate were obtained from Fisher Scientific, USA and used as received. The AMC-2 catalyst was purchased from Aerojet Chemicals, California, US. Epon 828 (epoxy equivalent weight, EEW 185-192 g/eq. Hexion technical data sheet of Epon 828 issued September 2005) and Epon 1001F (EEW 525-550 g/eq.
It is understood the mechanism is acid-catalyzed where protons coordinate with the carbonyl oxygen to make the carbonyl carbon more electropositive for nucleophilic attack (Scheme 1). In the experimental procedure all reactants were added together, this is inefficient as the protons can coordinate with either trans-cinnamic acid or methanol. Coordination with methanol is unnecessary as it reduces its nucleophilicity and makes less protons available to coordinate with the carboxylic acid. To improve
RESULTS & DISCUSSION The reaction scheme for the oxidation of cyclohexene to adipic acid is shown in Figure 2. This reaction was an ionic addition reaction, and it utilized the oxidizing properties of H2O2 in the presence of WO42-. For this reaction to occur, first Na2WO4 dissociated in the aqueous layer due to its ionic properties and the polarity of water as the solvent. WO42-, a complex stabilized by its resonance contributors, was taken into the organic layer by Aliquat 336, the phase transfer catalyst.
Generally speaking, Friedel-Craft acylation could be useful in a practical application such as industrial chemistry. Using this reaction mechanism can create plastic, synthetic rubber and ethylbenzene, which can eventually lead to polystyrene (Chemical Technology). This reaction can also synthesize high-octane gasoline, commonly referred to as “premium gas.” Therefore, the products generated from Friedel-Crafts acylation are significant because they are used in everyday
Purpose This experiment is to determine the concentration of the solute copper sulfate pentahydrate, and the unknown solution, by passing different wavelengths of light through each solution. Procedure Weigh out approximately 5g of copper sulfate pentahydrate. Record the mass and place the solute into a 50 mL volumetric flask. Fill half of the flask with distilled water, add the stopper for the flask, and lightly shake the flask, until the copper sulfate pentahydrate fully dissolved.