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By Robert Martin, Jean-Pierre Buisson

An vital source for the synthesis of intermediates of strong point chemical substances, prescription drugs and high-quality chemical compounds. fragrant Hydroxyketones from Butanone to Dotriacontanone presents the reader with exhaustive details overlaying constitution, instruction, physicochemical features, in addition to a comparable bibliography. The guide is gifted in dictionary variety, with a logical class of the ketones, making the knowledge simply to be had for session. The publication is geared toward these operating in examine, improvement and construction purposes in a variety of industries (chemistry, pharmacy, cosmetics, paints and perfumes).

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Extra info for Aromatic Hydroxyketones: Preparation & Physical Properties: Aromatic Hydroxyketones from Butanone (C4) to Dotriacontanone (C32)

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226–227 [1159]. C16H14Cl2N4O5 mol. wt. 22 1 Aromatic Hydroxyketones Derived from 1-Butanoic Acid 25 1-(3,5-Dichloro-4-hydroxyphenyl)-1-butanone [129527-09-9] C10H10Cl2O2 OH Cl Cl CO(CH2)2CH3 Synthesis -Obtained by Fries rearrangement of 2,6-dichlorophenyl butyrate with aluminium chloride for 1 h at 140–150 (59 %) [3079]. p. 96–97 [3079]. [129527-10-2] Na salt mol. wt. 10 C10H9Cl2O2Na mol. wt. 07 1-(4,5-Dichloro-2-hydroxyphenyl)-1-butanone [71290-02-3] OH CO(CH2)2CH3 Cl C10H10Cl2O2 mol. wt. 10 Synthesis -Obtained by condensation of butyryl chloride on 3,4-dichlorophenol [2958].

Wt. 28 -Obtained by reaction of acetic anhydride with resbutyrophenone in the presence of pyridine [2384]. p. 15 170–175 [2384]. C24H20O5 Dibenzoate mol. wt. 42 -Obtained by reaction of benzoyl chloride with resbutyrophenone in the presence of pyridine. The mixture was heated on a boiling water bath for 3 h [2384]. 25 210 [2384]. C24H24O3 Dibenzyl ether mol. wt. p. 61–62 [2181]. Dimethyl ether [6703-00-0] C12H16O3 mol. wt. 26 -Obtained by Friedel-Crafts reaction of butyric anhydride with resorcinol dimethyl ether in the presence of Hf[N(SO2C8H17)2]4 in chlorobenzene and SV135 at 70 for 2 h (96 %) [1245].

Wt. p. 134 [1449]. BIOLOGICAL ACTIVITY: Glycosuric [1449]; Toxicity [1449]. 1-(5-Amino-2,4-dihydroxyphenyl)-1-butanone C10H13NO3 OH CO(CH2)2CH3 HO mol. wt. 22 Synthesis -Refer to: [166]. Dimethyl ether [100370-41-0] C12H17NO3 mol. wt. 27 NH2 -Obtained from 2,4-dimethoxy-5-nitrobutyrophenone by treatment with clean mossy zinc and HCl on the water bath (52 %) [166]. p. 75–76 [166]. 1-[5-Bromo-2,4-dihydroxy-3-(1-oxobutyl)]benzoic acid [99853-34-6] C11H11BrO5 OH CH3(CH2)2CO HO Br mol. wt. 11 Syntheses CO2H -Obtained by adding butyric anhydride to a cold solution of methyl 2,4-dihydroxy5-bromobenzoate and aluminium chloride in nitrobenzene.

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