Butyl acetate carbonate

Helium Hydrogen Butene Butyl acetate Carbon monoxide, methane Hydrogen... 

Polystyrene Toluene, chloroform, cyclohexanone, butyl acetate, carbon disulfide Lower alcohols, diethyl ether (swells)... 

Acetone, butyl acetate, carbon tetrachloride, diisobutyl ketone, hexane, methyl ethyl ketone, methyl isobutyl ketone, nitropropane, toluene, xylene... 

The literature data and our own experience indicate that drying with a molecular sieve can be employed with good results for the following solvents acetone, acetonitrile, benzene, butane, butyl acetate, carbon tetrachloride, dichloroethane, cyclohexane, diethyl ether, dimethylformamide, dimethyl sulphoxide, ethanol, heptane, isopropanol, di-isopropyl ether, pyridine, toluene and xylene. 

Acetic Anhydride Acetone Acetyl Bromide Acetyl Chloride Ammonium Hydroxide Amyl Acetate Aromatic Hydrocarbons Butyl Acetate Carbon Bisulfide... 

Ethylene/butyl acetate/carbon monoxide copolymer... 

Hydrolysis (or saponification) of n-butyl acetate. Boil 4-5 g. of n-butyl acetate (Section 111,95) with 50 ml. of 10 per cent, sodium hydroxide solution under reflux until the odour of the ester can no longer be detected (about 1 hour). Set the condenser for downward distiUation and coUect the first 10 ml. of distillate. Saturate it with potassium carbonate, aUow to stand for 5 minutes, and withdraw all the Uquid into a small pipette or dropper pipette. AUow the lower layer of carbonate solution to run slowly into a test-tube, and place the upper layer into a small test-tube or weighing bottle. Dry the alcohol with about one quarter of its buUr of anhydrous potassium carbonate. Remove the alcohol with a dropper pipette and divide it into two parts use one portion for the determination of the b.p. by the Siwoloboff method (Section 11,12) and convert the other portion into the 3 5-dinitrobenzoate (Section III, 27) and determine the m.p. 

Successful results have been obtained (Renfrew and Chaney, 1946) with ethyl formate methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec.-butyl and iso-amyl acetat ethyleneglycol diacetate ethyl monochloro- and trichloro-acetates methyl, n-propyl, n-octyl and n-dodecyl propionates ethyl butyrate n-butyl and n-amyl valerates ethyl laurate ethyl lactate ethyl acetoacetate diethyl carbonate dimethyl and diethyl oxalates diethyl malonate diethyl adipate di-n-butyl tartrate ethyl phenylacetate methyl and ethyl benzoates methyl and ethyl salicylates diethyl and di-n-butyl phthalates. The method fails for vinyl acetate, ieri.-butyl acetate, n-octadecyl propionate, ethyl and >i-butyl stearate, phenyl, benzyl- and guaicol-acetate, methyl and ethyl cinnamate, diethyl sulphate and ethyl p-aminobenzoate. 

Acetone with benzene, butyl acetate, butyl alcohol, carbon tetrachloride, chloroform, cyclohexane, ethanol, ethyl acetate, methyl acetate, acetonitrile, petroleum ether or water. 

Discussion. Sodium diethyldithiocarbamate (B) reacts with a weakly acidic or ammoniacal solution of copper(II) in low concentration to produce a brown colloidal suspension of the copper(II) diethyldithiocarbamate. The suspension may be extracted with an organic solvent (chloroform, carbon tetrachloride or butyl acetate) and the coloured extract analysed spectrophotometrically at 560 nm (butyl acetate) or 435 nm (chloroform or carbon tetrachloride). 

In the presence of a strong base, the ot carbon of a carboxylic ester can condense with the carbonyl carbon of an aldehyde or ketone to give a P-hydroxy ester, which may or may not be dehydrated to the a,P-unsaturated ester. This reaction is sometimes called the Claisen reaction,an unfortunate usage since that name is more firmly connected to 10-118. In a modem example of how the reaction is used, addition of tert-butyl acetate to LDA in hexane at -78°C gives the lithium salt of ferf-butyl acetate, " (12-21) an enolate anion. Subsequent reaction a ketone provides a simple rapid alternative to the Reformatsky reaction (16-31) as a means of preparing P-hydroxy erf-butyl esters. It is also possible for the a carbon of an aldehyde or ketone to add to the carbonyl carbon of a carboxylic ester, but this is a different reaction (10-119) involving nucleophilic substitution and not addition to a C=0 bond. It can, however, be a side reaction if the aldehyde or ketone has an a hydrogen. 

Ethyl acetate, v, 2 butyl acetate, v, 2 propyl formate, v, 4 dimethyl carbonate, 1, 1 ... 

Ethyl tert-butyl malonate has been prepared by adding tert-butyl acetate and ethyl carbonate to sodium triphenylmethyl,3 and from ethyl malonyl chloride and fer/-butyl alcohol.4 The present procedure is an adaptation of that for the preparation of di-fer(-butyl malonate.2... 

The /V -hydroxylamino compounds (404) and (405), obtained from the reaction of tert-butyl acetate with 3,4-dihydroisoquinoline-A-oxide or 5,5-dimethyl-pyrroline-/V-oxide, when boiled in methylene chloride in the presence of triphenylphosphine, carbon tetrachloride and triethylamine, are transformed to (1,2,3,4- tetrahydroisoquinolin-l-ilidene) acetate (406) or (pyrrolidin-2-ilidene) acetate (407) (Scheme 2.181) (645). 

Prior to the actual metathesis event, coupling of 13 and 28 via an ester linkage was required (Scheme 2.3). Two methods were employed in this connection. The first involved the aforementioned two-carbon expansion of aldehyde 28. Thus, condensation of 28 with Rathke anion (lithiated tert-butyl acetate) generated a mixture of dia-stereomeric alcohols the major product was shown to have the requisite 3S configuration. TBS protection of ester 29 and subsequent ester hydrolysis generated the desired add, 31, which could be further esterified with alcohol 13 in 78 % yield. 

Bromine (dry gas) Bromine (liquid) Bromobenzene Butanol Butyl acetate Butylamine Butylchloride Butyric acid Calcium chloride Carbon tetrachloride Castor oil Cellosolve Cellosolve acetate Chlorine (dry gas) Chlorine water Chloroacetic acid Chlorobenzene Chloroform Chlorosulfonic acid Chromic acid Citric acid Colza oil Copper sulfate Cyclohexane Cyclohexanol Cyclohexanone... 

A variety of other carbon nucleophiles have been alkylated with alcohols including malonate esters, nitroaUcanes, ketonitriles [119, 120], barbituric acid [121], cyanoesters [122], arylacetonitriles [123], 4-hydroxycoumarins [124], oxi-ndoles [125], methylpyrimidines [126], indoles [127], and esters [128]. Selected examples are given in Scheme 35. Thus, benzyl alcohol 15 could be alkylated with nitroethane 147, 1,3-dimethylbarbituric acid 148, phenylacetonitrile 149, methyl-pyrimidine 150, and even f-butyl acetate 151 to give the corresponding alkylated products 152-156. 

Degradation of methyl terf-butyl ether by bifunctional aluminum in the presence of oxygen was investigated by Lien and Wilkin (2002). Bifunctional aluminum was synthesized by sulfating aluminum metal with sulfuric acid. When the initial methyl terf-butyl ether concentration was 14.4 mg/L, 90% of methyl ferf-butyl ether degraded within 24 h forming acetone, methyl acetate, tert-hniyX alcohol, and ferf-butyl formate. Carbon disulfide was tentatively identified as a reaction product by GC/MS. Product yields were 27.6% for acetone, 18.4% for methyl acetate, 21% for tert-hniyX alcohol, and 6.1% ferf-butyl formate. When the initial concentration of methyl tert-butyl ether was reduced to 1.4 mg/L, 99.5% of methyl terCbutyl ether reacted. Yields of acetone, methyl acetate, and /erf-butyl alcohol were 54.7,17.2, and 13.2, respectively. 

The Michael additions of various carbon nucleophiles such as cyanide [15b, 22b], anions generated from nitromethane [27], ferf-butyl acetate [9], malon-ates [27] and O Donnell s glycine equivalent [541, cuprates [9,15b] or Grignard reagents [53] under copper catalysis [55] have also been reported (Scheme 24). 

The mechanism of transport of GPG using SLM has been studied at the authors laboratory [56]. GPG could be permeated from alkaUne feed of carbonate buffer into an acidic stripping solution of acetate buffer across the membrane comprising Aliquat-336 in -butyl acetate immobiUzed in a polypropylene (Gelgard 2400) support. The transport mechanism is a case of counter transport exhibiting overall rate dependence on solute diffusion in the membrane phase as well as the mass transfer across the aqueous boundary films. 

Oils Edible Safflower Potassium Binoxalate Ammonium Chloride Salicylic Acid Ammonium Chloride Lead Acetate Potassium Binoxalate Sodium Silicofluoride Ammonium Carbonate Fluocilicic Acid P-Dichlorobenzene Ammonium Phosphate Sec-Butyl Acetate Sec-Butyl Alcohol Calcium Phosphate Selenium Trioxide Selenium Dioxide Selenium Dioxide Selenium Dioxide Selenium Trioxide Antimony Trioxide Calcium Hypochlorite Carbaryl Cyclohexanone Charcoal... 

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