Methyl 4- butyrate

Methyl formate. Ethyl formate Methyl acetate Iso-propyl formate Ethyl acetate Methyl propionate "-Propyl formate Iso-propyl acetate Methyl iso-butyrate Iso-butyl formate. Ethyl propionate M-Propyl acetate. Methyl butyrate. ... [Pg.544]

Methylsuccinic acid has been prepared by the pyrolysis of tartaric acid from 1,2-dibromopropane or allyl halides by the action of potassium cyanide followed by hydrolysis by reduction of itaconic, citraconic, and mesaconic acids by hydrolysis of ketovalerolactonecarboxylic acid by decarboxylation of 1,1,2-propane tricarboxylic acid by oxidation of /3-methylcyclo-hexanone by fusion of gamboge with alkali by hydrog. nation and condensation of sodium lactate over nickel oxide from acetoacetic ester by successive alkylation with a methyl halide and a monohaloacetic ester by hydrolysis of oi-methyl-o -oxalosuccinic ester or a-methyl-a -acetosuccinic ester by action of hot, concentrated potassium hydroxide upon methyl-succinaldehyde dioxime from the ammonium salt of a-methyl-butyric acid by oxidation with. hydrogen peroxide from /9-methyllevulinic acid by oxidation with dilute nitric acid or hypobromite from /J-methyladipic acid and from the decomposition products of glyceric acid and pyruvic acid. The method described above is a modification of that of Higginbotham and Lapworth. ... [Pg.56]

Methyl-l -butene N-Methylbutylamine Methyl butyl ketone Methyl butyrate Methyl cellosolve Methyl cellosolve acetate Methyl chloride... [Pg.210]

Write equations to show the formation of the esters, methyl butyrate and butyl propionate. [Pg.349]

R+ is intense in methyl acetate, methyl propionate, methyl butyrate, and methyl pentanoate. [Pg.63]

Isobutyl fomtafe Propyl acetate isopropyl acetate Ethyl propionate Methyl butyrate Methyl isobutyrate Diethyl carbohale Edtyl lactate 2-Methoxyethyl acetate... [Pg.474]

N-VALERIC ACID ISOBUTYL FORMATE N-PROPYL ACETATE ETHYL PROPIONATE METHYL BUTYRATE METHYL ISOBUTYRATE PIPERIDINE N-PENTANE 2-METHYL BUTANE 2 2-DIMETHYL PROPANE... [Pg.946]

Cyclization of ethyl 3-cyano-3-methyl butyrate 201 with hydrazine hydrate gave the hydrazonopyridazine 202, which underwent ring closure with oxalyl chloride to give (85MIP1) pyridazinotriazine derivative 203. [Pg.235]

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