Basf Aktiengesellschaft

Bernd Meissner

Werner Fliege

Christian Dudeck

Hans Diem

Karl-Heinz Ross

Gunter Lehmann

Norbert Petri

Hans Diehm

Peter Horn

Werner Hoffmann

Leopold Hupfer

Walter Gramlich

Axel Nissen

Roman Fischer

Harald Laas

Wolfgang Koernig

Juergen Paetsch

Fritz Brunnmueller

Wolfgang Sauer

Otto Woerz

Gernot Teege

Wolfgang Muehlthaler

Frank Weiss

3,6-Dimethyl-3-hydroxy-oct-1-ynes and -oct-1-enes and their esters with lower alkanoic acids, of the general formula I ##STR1## where X and Y are H or the two X's and/or the two Y's together are a further bond between the carbon atoms on which they are present, and R is H, --CO--CH.sub.3, --CO--C.sub.2 H.sub.5 or --CO--C.sub.3 H.sub.7, their use as scents, and a process for the preparation of 3,6-dimethyl-3-hydroxy-octane. The novel compounds exhibit interesting, predominantly floral, woody, herbal and fruity notes. The alcohols of the formula I are of particular importance because they serve as intermediates for a novel and particularly advantageous method of obtaining 3,6-dimethyl-3-hydroxy-octane, a compound required in large amounts as a fragrance for soaps and detergents.

3,6-Dimethyl-3-hydroxy-oct-1-ynes and -oct-1-enes, derivatives of these,

In a process for the preparation of a carboxylic acid ester of .beta.-formyl-crotyl alcohol by rearrangement of the corresponding carboxylic acid ester of 2-formyl-2-hydroxy-but-3-ene or of an acetal or acylate thereof in the presence of copper or a copper compound, followed, where relevant, by hydrolytic cleavage of the acetal or acylate, more especially in the preparation of 4,4-dimethoxy-3-methyl-crotyl acetate, the yield is improved by carrying out the rearrangement in the presence of copper (I) chloride as the catalyst and ensuring that low-boiling by-products formed during the rearrangement are removed. The products are of great importance as starting materials for an industrial synthesis of vitamin A and its derivatives.

Process for the preparation of carboxylic acid esters of

Diketones are prepared by oxidizing glycols in the presence of a silver catalyst and/or copper catalyst of a specific particle size, under specific temperature conditions and with a specific composition of the catalyst. The end products are starting materials for the preparation of dyes, drugs, plastics, scents, wrinkle-resist finishes and assistants for increasing the tear strength and resilience of fibrous materials, hardeners for use in the photographic industry, textile assistants for preventing shrinkage after washing, and paper assistants.

Preparation of diketones

Aliphatic hydroxycarbonyl compounds etherified with aliphatic groups are prepared by oxidizing hydroxyalcohols in the presence of a metal catalyst which consists of one or more layers, each of a particular weight and each containing particles of a particular size, the catalyst bed also having a particular total thickness, and the catalyst components used being silver and copper, with or without added copper/tin/phosphorus or silver alone. The etherified hydroxyaldehydes and hydroxyketones obtainable by the process of the invention are valuable starting materials for the preparation of dyes, pesticides, plastics and scents.

Manufacture of aliphatic hydroxycarbonyl compounds etherified with

Alkyl pyruvates are prepared by oxidizing alkyl lactates in the presence of a silver catalyst of a defined particle size, at from 450.degree. to 700.degree. C. The products are starting materials for the preparation of drugs, synthetic resins and plastics.

Preparation of alkyl pyruvates

3-Methyl-2-buten-1-al is prepared by isomerizing 3-methyl-3-buten-1-al in the presence of acidic or basic compounds. The product is a starting material for the manufacture of dyes, pesticides, pharmaceuticals, plastics and scents.

Preparation of 3-methyl-2-buten-1-al

4-(m,m'-ditert.-butyl-p-hydroxyphenyl)-butan-2-ones are produced by reaction of a 4-hydroxybutanone-(2) with 2,6-ditert.-butylphenol in the presence of a strong acid at elevated temperature. The compounds obtainable by the process, particularly 4-(m,m'-ditert.-butyl-p-hydroxyphenyl)-butane-2-one, are starting materials for the production of dyes, pest control agents and plastics auxiliaries and particularly of stabilizers for polyolefins and polyamides.

Production of 4-(m,m'-ditert.-butyl-p-hydroxyphenyl)-butan-2-ones

3-Alkyl-buten-1-als are prepared by oxidative dehydrogenation of 3-alkyl-buten-1-ols in the presence of a silver catalyst, of a particular total thickness, comprising 2 or more layers each of a particular weight and containing particles of a particular size. The products are starting materials for the manufacture of dyes, pesticides, drugs, plastics, naturally occurring materials and scents.

Preparation of 3-alkyl-buten-1-als

New bis-[4-(m,m'-di-tert.-butyl-p-hydroxyphenyl)-butyl-(2)] dicarboxylic acid esters which are starting materials for the manufacture of dyes, pesticides and additives for plastics, especially stabilizers for polyolefins and polyamides, and are themselves stabilizers, aging retardants or antioxidants for organic products.

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Heidelberg, Germany

Bernd Meissner