Journal of the Chemical Society, Part 2The Society., 1959 |
From inside the book
Results 1-3 of 72
Page 1533
... obtained from the filtrate . Similarly , the octyl ester ( 7 · 6 g . , 1 mol . ) gave boric acid ( 1.84 g . , 97 % ) ; catechol ( 2 · 9 g . , 86 % ) , m . p . and mixed m . p . 105 ° , was obtained by evaporation of the solvent and ...
... obtained from the filtrate . Similarly , the octyl ester ( 7 · 6 g . , 1 mol . ) gave boric acid ( 1.84 g . , 97 % ) ; catechol ( 2 · 9 g . , 86 % ) , m . p . and mixed m . p . 105 ° , was obtained by evaporation of the solvent and ...
Page 1588
... obtained from the ozonolysis product as ammonia . Further evidence for structure ( I ; R : Me ) was obtained by treating the corresponding methiodide with alkali ; the anhydro - base , identical with Ciamician's base C10H17N referred to ...
... obtained from the ozonolysis product as ammonia . Further evidence for structure ( I ; R : Me ) was obtained by treating the corresponding methiodide with alkali ; the anhydro - base , identical with Ciamician's base C10H17N referred to ...
Page 2077
... obtained by another route.4 Pyrolysis of n - butyl p - methoxyphenylchloroboronite ( II ) did not result in fission of the methoxy - group , but in slow formation of p - methoxyphenylboronic anhydride ( see ref . 5 for similar reactions ...
... obtained by another route.4 Pyrolysis of n - butyl p - methoxyphenylchloroboronite ( II ) did not result in fission of the methoxy - group , but in slow formation of p - methoxyphenylboronic anhydride ( see ref . 5 for similar reactions ...
Contents
Potentially tautomeric pyridines Part II 2 3 and 4Acetamido and benz | 1317 |
ABEL E W and Wilkinson G 1501 | 1324 |
The second rapid step in the nucleophilic substitution of alkyl halides Part I | 1327 |
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absorption acetic acid acetic anhydride acetone added alcohol alumina Amer amine anhydride anhydrous atom band benzene benzyl boiling bond bromide Calc carbon carboxylic CH₂ Chem chloride chloroform chromatography complex compound concentration constant crystals cyclic decomp derivatives dilute dioxan dissolved distilled dried elution ester ethanol ethyl acetate ethylene evaporated filtered formed Found fraction gave give H₂O halides heated hydrochloric acid hydrogen hydrogen chloride hydrolysis hydroxide infrared iodide ionic isolated ketone light petroleum b. p. lithium lithium aluminium hydride m. p. and mixed methyl mixed m. p. mixture mole molecular molecule needles nitrogen obtained oxide phenol phosphate picrate polymer potassium potassium hydroxide precipitate prepared prisms pyridine reaction reduced refluxed requires residue room temperature salt sodium hydroxide solid solvent spectra spectrum structure sulphate sulphuric acid Table tetrachloride values washed yellow yield