Benzyl acetone

Acetic Anhydride Acetone Benzyl Chloride Ethyl Ether HCI (Gas)... 

Styphnic acid. Ammonia, Barium chlorate dehydrate. Acetone Benzyl chloride. Sodium cyanide. Ethyl alcohol. Liquid hromine, Carhon tetrachloride. Sodium hydroxide. Sodium sulfate. Chloroform... 

Polyester Phenols, nitrated hydrocarbons, acetone, benzyl alcohol Esters, alcohols, hydrocarbons... 

Benzylacetone. See Benzylidene acetone Benzyl acetyl acetate. See Benzyl acetoacetate Benzyl alcohol... 

Benzyl butyl ether Benzyl butyrate Benzyl cinnamate Benzyl 2,3-dimethylcrotonate Benzyl dipropyl ketone Benzyl disulfide Benzyl ether Benzyl ethyl ether Benzyl formate Benzylidene acetone Benzyl isobutyrate Benzyl isovalerate Benzyl mercaptan Benzyl methoxyethyl acetal Benzyl phenylacetate Benzyl propionate Benzylsalicylate Birch (Betula pendula) tar oil DL-Bomeol Bomyl acetate... 

Benzyl ether Benzyl ethyl ether Benzyl formate Benzylidene acetone Benzyl isobutyrate... 

N-PbeSTl-N.N. dlbenzyl-bydrazin 16 1166, CuminM-K-naphthylhydTazon 16, 563. Aceton.[benzyl-fl-napnthyI.hydiazon]... 

Chemicals causing environmental stress cracking list acetone, benzyl alcohol, carbon tetrachloride, cyclohexanone, nitrobenzene Wang, H T Pan, Q G Du, Q C Li, Y Q, Polym. Test., 22, 125-28, 2003. 

Generation of asymmetric ketenes in the photolysis of the chromium aminocarbene complex 253, in the presence of acetone benzyl imine, afforded the /S-lactames 254 with a modest level of asymmetric induction (70 % de) °. ... 

Benzyl N-carbobenzoxy-O-tosyl-L-serinate allowed to react with Na-benzyl-selenolate in dimethylformamide-acetone benzyl N-carbobenzoxy-Se-benzyl-L-selenocysteinate. Y 89%. F. e. s. D. Theodoropoulos, I. L. Schwartz, and R. Walter, Tetrah. Let. 1967, 2411 Biochemistry 6, 3927 (1967). 

Add in turn benzyl chloride (8 3 g., 8 o ml.) and powdered thiourea (5 gm.) to 10 ml. of 95% ethanol in a 100 ml. flask fitted with a reflux condenser. Warm the mixture on the water-bath with gentle shaking until the reaction occurs and the effervescence subsides then boil the mixture under reflux for 30 minutes. Cool the clear solution in ice-water, filter off the crystalline deposit of the benzylthiouronium chloride at the pump, wash it with ice-cold ethyl acetate, and dry in a desiccator. Yield, 11-12 g., m.p. 170-174°. The white product is sufficiently pure for use as a reagent. It is very soluble in cold water and ethanol, but can be recrystallised by adding ethanol dropwise to a boiling suspension in ethyl acetate or acetone until a clear solution is just obtained, and then rapidly cooling. 

The dibenzyl ketone has a very high b.p. (ca. 200°/21 mm.) and this remains in the flask when the unsymmetrical ketone has been removed by distillation. The dialkyl ketone has a comparatively low b.p. and is therefore easily removed by fractionation under normal pressure acetone is most simply separated by washing with water. In this way methyl benzyl ketone (R = CHj), ethyl benzyl ketone (R = CHgCH,) and n-propyl benzyl ketone (R = CHjCHjCH,) are prepared. By using hydrocinnamic acid in place of phenylacetic acid ... 

The suitability of the model reaction chosen by Brown has been criticised. There are many side-chain reactions in which, during reaction, electron deficiencies arise at the site of reaction. The values of the substituent constants obtainable from these reactions would not agree with the values chosen for cr+. At worst, if the solvolysis of substituted benzyl chlorides in 50% aq. acetone had been chosen as the model reaction, crJ-Me would have been —0-82 instead of the adopted value of —0-28. It is difficult to see how the choice of reaction was defended, save by pointing out that the variation in the values of the substituent constants, derivable from different reactions, were not systematically related to the values of the reaction constants such a relationship would have been expected if the importance of the stabilization of the transition-state by direct resonance increased with increasing values of the reaction constant. 

Benzylic halides resemble allylic halides m the readiness with which they form carbocations On comparing the rate of S l hydrolysis m aqueous acetone of the fol lowing two tertiary chlorides we find that the benzylic chloride reacts over 600 times faster than does tert butyl chloride... 

From cumene Almost all the phenol produced in the United States is prepared by this method Oxi dation of cumene takes place at the benzylic posi tion to give a hydroperoxide On treatment with dilute sulfuric acid this hydroperoxide is converted to phenol and acetone... 

A typical phenol plant based on the cumene hydroperoxide process can be divided into two principal areas. In the reaction area, cumene, formed by alkylation of benzene and propylene, is oxidized to form cumene hydroperoxide (CHP). The cumene hydroperoxide is concentrated and cleaved to produce phenol and acetone. By-products of the oxidation reaction are acetophenone and dimethyl benzyl alcohol (DMBA). DMBA is dehydrated in the cleavage reaction to produce alpha-methylstyrene (AMS). 

Riboflavin forms fine yellow to orange-yeUow needles with a bitter taste from 2 N acetic acid, alcohol, water, or pyridine. It melts with decomposition at 278—279°C (darkens at ca 240°C). The solubihty of riboflavin in water is 10—13 mg/100 mL at 25—27.5°C, and in absolute ethanol 4.5 mg/100 mL at 27.5°C it is slightly soluble in amyl alcohol, cyclohexanol, benzyl alcohol, amyl acetate, and phenol, but insoluble in ether, chloroform, acetone, and benzene. It is very soluble in dilute alkah, but these solutions are unstable. Various polymorphic crystalline forms of riboflavin exhibit variations in physical properties. In aqueous nicotinamide solution at pH 5, solubihty increases from 0.1 to 2.5% as the nicotinamide concentration increases from 5 to 50% (9). 

When exposed to ait, the sodium salts tend to take up moisture and form dihydrates. The alkah metal xanthates are soluble ia water, alcohols, the lower ketones, pyridine, and acetonitrile. They are not particularly soluble ia nonpolar solvents, eg, ether or ligroin. The solubiUties of a number of these salts are Hsted ia Table 4. Potassium isopropyl xanthate is soluble ia acetone to ca 6 wt %, whereas the corresponding methyl, ethyl, / -propyl, n-huty isobutyl, isoamyl, and benzyl [2720-79-8] xanthates are soluble to more than 10 wt % (12). The solubiUties of the commercially available xanthates ia water are plotted versus temperature ia Figure 1 (14). 

Ethylenediamine (70,71), benzyl alcohol and acetone (72), ethylene glycol (73) and C2—C g carboxyUc acids (74) are claimed to increase the reactivity of cellulose toward acetylation. Sodium hydroxide and Hquid ammonia (71) are excellent swelling agents and have been used to activate cellulose before esterification. Ultrasonic treatment of cellulose slurries (75) reportedly swells the fibers and improves reactivity. 

Mel, K2CO3, acetone, reflux, 6 h. This is a veiy common and often veiy efficient method for the preparation of phenolic methyl ethers it is also applicable to the. formation of phenolic benzyl ethers. 

This method is particularly applicable to the more reactive benzyl halides which are easily hydrolyzed in the aqueous media usually employed for the metathetical reaction with alkali cyanides. For example, anisyl chloride treated with sodium cyanide in aqueous dioxane gives, as a by-product, 5-10% of anisyl alcohol as determined by infrared analysis. The use of anhydrous acetone not only prevents hydrolysis to the alcohol but also decreases the formation of isonitriles. This method was also applied successfully by the submitters to the preparation of -chlo-rophenylacetonitrile in 74% yield. 

The thenyl chlorides appear to be more reactive in nucleophilic aliphatic substitution than the benzyl analogs. Thus, 2-thenyh chloride gives, in the reaction with sodium cyanide in ethanol, a mixture of ethyl 2-thenyl ether (25% yield) and 2-thenyl cyanide (32% yield), whereas benzyl chloride gives a high 3deld of benzyl cyanide uncontaminated with benzyl ether. When 2-thenyl chloride and benzyl chloride were allowed to compete for a deficiency of sodium amyloxide, 2-thenyl chloride reacted three times faster. In acetone solution 2-thenyl cyanide is obtained smoothl. ... 

Cyclic hydroxamic acids and V-hydroxyimides are sufficiently acidic to be (9-methylated with diazomethane, although caution is necessary because complex secondary reactions may occur. N-Hydroxyisatin (105) reacted with diazomethane in acetone to give the products of ring expansion and further methylation (131, R = H or CH3). The benzalphthalimidine system (132) could not be methylated satisfactorily with diazomethane, but the V-methoxy compound was readil3 obtained by alkylation with methyl iodide and potassium carbonate in acetone. In the pyridine series, 1-benzyl-oxy and l-allyloxy-2-pyridones were formed by thermal isomeriza-tion of the corresponding 2-alkyloxypyridine V-oxides at 100°. 

Alkylation at the ind-N of l,2,3,4-tetrahydro-j8-carbolines has been carried out with alkyl halide after treatment with sodamide in the usual manner. Cyanoethylation of a p /r-V-substituted tetrahydro-jS-carboline in the presence of Triton B yields the corresponding 9-cyanoethyl derivative. Similarly, treatment of p / -V-methyl-l,2,3,4,4a,9b-hexahydro-y-carboline with sodamide, followed by benzyl chloride, leads to the ind-A -benzyl-substituted derivatives. l-Oxo-l,2,3,4-tetrahydro-j8-carboline yields the ind-A -methyl derivative directly with dimethyl sulfate.Prolonged treatment with sodium hydride, followed by methyl iodide, yields the 2,9-dimethyl derivative. Heating with sodium hydride in acetone followed by the addition of dimethyl sulfate gives rise to the ind-V-methyl derivative. ... 

Differences in solubility of the reactants may for example be utilized as follows. Sodium iodide is much more soluble in acetone than are sodium chloride or sodium bromide. Upon treatment of an alkyl chloride or bromide with sodium iodide in acetone, the newly formed sodium chloride or bromide precipitates from the solution and is thus removed from equilibrium. Alkyl iodides can be conveniently prepared in good yields by this route. Alkyl bromides are more reactive as the corresponding chlorides. Of high reactivity are a-halogen ketones, a-halogen carboxylic acids and their derivatives, as well as allyl and benzyl halides. 

Ni prior to use by refluxing it for 3 h with acetone, in order to suppress hydrogenolysis of the benzylic protecting groups (51). 

First, dimethylamino-2-phenoxyethane was made by reacting chloro-2-phenoxyethane with dimethylamine. Benzyl chloride (10 grams) was then added to a solution of 1-dimethylamino-2-phenoxyethane (12.3 grams) in acetone (35 ml). The mixture warmed spontaneously and N-benzyl-N,N-dimethyl-N-2-phenoxyethylammonium chloride slowly crystallized. After 24 hours, this solid was filtered off, washed with fresh acetone and dried immediately in vacuo, MP 135°-136°C. 

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