Oxalic diethyl ester

Dimethyl peroxide Diethyl peroxide Di-t-butyl-di-peroxyphthalate Difuroyl peroxide Dibenzoyl peroxide Dimeric ethylidene peroxide Dimeric acetone peroxide Dimeric cyclohexanone peroxide Diozonide of phorone Dimethyl ketone peroxide Ethyl hydroperoxide Ethylene ozonide Hydroxymethyl methyl peroxide Hydroxymethyl hydroperoxide 1-Hydroxyethyl ethyl peroxide 1 -Hydroperoxy-1 -acetoxycyclodecan-6-one Isopropyl percarbonate Isopropyl hydroperoxide Methyl ethyl ketone peroxide Methyl hydroperoxide Methyl ethyl peroxide Monoperoxy succinic acid Nonanoyl peroxide (75% hydrocarbon solution) 1-Naphthoyl peroxide Oxalic acid ester of t-butyl hydroperoxide Ozonide of maleic anhydride Phenylhydrazone hydroperoxide Polymeric butadiene peroxide Polymeric isoprene peroxide Polymeric dimethylbutadiene peroxide Polymeric peroxides of methacrylic acid esters and styrene... [Pg.163]

Acetic acid, methyl ester Acetic acid, ethyl ester Pentanoic acid, methylethyl ester Acetic acid, methylethyl ester Acetic acid, 3-propenyl ester Acetic acid, benzyl ester Oxalic acid, dimethyl ester Oxalic acid, diethyl ester Oxalic acid, fe(l-methylethyl) ester... [Pg.368]

It is worthy of note that the melting points of the methyl esters are generally higher than those of the corresponding ethyl esters thus, to take a well-known example, dimethyl oxalate (melting point 54°) is a solid whilst the diethyl ester is a liquid. [Pg.145]

Diethyl oxalate Oxalic acid, diethyl ester (8) Ethanedioic acid, diethyl ester (9) (95-92-1)... [Pg.68]

Organoaluminum compounds, reaction with imino carbocations, 66, 189 Orthoester Claisen rearrangement, 66, 22 Orthoformic acid, triethyl ester, 65, 146 Oxalic acid, diethyl ester, 65, 146... [Pg.255]

This class of compound is represented by the dicyanoiodate(I) anion, involving a pseudohalide rather than an alkyl or aryl ligand. The linear ion, with I—C distance of 2.302 A, has been characterized in the compound K[I(CN)2]C6H12N202, resulting from reaction of an aqueous solution of KCN with an ethanolic solution of ICN. The diimino oxalic acid diethyl ester molecule apparently stabilizes the structure.56... [Pg.317]

SYNS DIETHYL ETHANEDIOATE ETHYL OXALATE ETHYL OXALATE (DOT) OXALIC ACID, DIETHYL ESTER... [Pg.494]

The Claisen condensation of diethyl oxalate with esters of fatty acids (cf. method 211) produces a-ethoxalyl esters which are thermally de-carbonylated to alkylmalonic esters. The over-all yields range from 78% to 91% for the conversion of fatry esters up to ethyl stearate. Phenyl-malonic ester is made in 85% yield. Powdered glass is sometimes used... [Pg.252]

Butane, 1-iodo 8.6 Oxalic acid, diethyl ester 12.6... [Pg.483]

OXALIC ACID, DIETHYL ESTER (95-92-1) Combustible liquid (flash point 168°F/ 76°C). Water slowly forms oxalic acid. Incompatible with zinc acetate. Violent reaction with strong oxidizers. [Pg.903]

Diethyl Oxalate, Ethanedioic acid diethyl ester ethyl oxalate diethyl ethanedio te oxalic acid diethyl ester. c[Pg.493]

Ethyl Oxalacetate. Oxobutanedioie add diethyl ester diethyl oxalacetate oxaloacetic ester. C Hl2Os mol wt 188.18. C 51,06%, H 6,43%. O 42.51%. C OOCCH CO-COOCjHj. Obtained by the action of sodium on a mixture of ethyl oxalate and ethyl acetate. [Pg.603]

Beilstein Handttook Reference) BRN 0606350 Diethyl ethanedloate Oiethylester kyseliny stavelove EINECS 202-464-1 Ethanedlolc acid, diethyl ester Ethyl oxalate HSDB 2131 NSC 8851 Oxalic acid, diethyl ester Oxalic ether UN2525. Used as a solvent and Intermediate In manufacture of chemicals and pharmaceuticals. Liquid mp = -40.6" bp = 185.7" d ° = 1.0785 poorly soluble in H2O, soluble in EtOH, Et20, Me2CO, CCU. [Pg.213]

Phenyl-2-oxobutyric acid was obtained either by selective hydrogenation of benzylidenepyruvic acid (5% Pd/C, EtOH, RT, 1 bar H2) [4b] or by condensation of ethyl 3-phenylprop-ionate with oxalic acid diethyl ester followed by hydrolysis and decarboxylation. In both cases. [Pg.140]

Carbon-11 can also be inserted into an aromatic ring Methyl chloroformate has been converted into carbon-11 labelled oxalic acid in a three-step synthesis. The first step (equation 75) was done in a water-dichloromethane mixture using tetrabutylammonium hydroxide and CN" under phase transfer catalysis conditions. The conversion to the diethyl ester and to the oxalic acid were done in high yields in 0.5 and 0.25 minute, respectively, in a microwave cavity. [Pg.657]

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