Abstract:
PURPOSE: To obtain the entitled sweetener sweetening food with satisfactory taste and flavor like cane sugar by including an artificial sweetener and desoxysugar. CONSTITUTION: The sweetener includes (A) at least one kind of artificial sweeteners such as acesulfam K, and (B) at least one kind of deoxysugar such as rhamnose, fucose. By mixing a small amount of the component B, intense similarity to cane sugar is given to obtain a sweetener useful for an artificial sweetener for a dining table.
Abstract:
Process for preparing aryl esters of phosphonous acid of formula (V), where A is non-existent or a direct bond or a divalent hydrocarbon bridge with 1 to 6 carbon atoms, which can be substituted by the groups mentioned below, or a heteroatom, cycloalkylidene with 4 to 8 carbon atoms or phenylalkylidene with 7 to 12 carbon atoms, n is equal to 1 or 2, R as a monovalent residue denotes certain non-aromatic or aromatic hydrocarbon residues, the aromatic residues denoting substituents such as alkyl, alkoxy, alkylthio, dialkylamino, aryl, aryloxy or halogen, and as a divalent residue denotes a phenylene or naththylene residue, which can carry non-aromatic hydrocarbon residues as substituents, R is a non-aromatic hydrocarbon residue with 1 to 18 carbon atoms, aryl, arylmethyl, arylethyl or arylisopropyl, each aryl containing 6 to 10 carbon atoms, and R denotes hydrogen or one of the groups mentioned under R . In a first stage a halogenated hydrocarbon R (-Hal)n, in which R has the above-mentioned meaning, n = 1 or 2, and the halogen has an atomic weight of at least 35, is converted under Grignard conditions with at least molar quantities of magnesium to the corresponding organomagnesium compounds R (MgHal)n. These are reacted in a second stage with phosphoric acid-bis-arylester halides of formula (VI), where R , R and Hal have the above-mentioned meanings, to form the phosphonous acid arylester (V). The invention also relates to a plastics moulding material, in particular a polyolefin moulding material, containing the phosphonous acid arylester of formula (V). The properties of the moulding material are superior to those of materials which contain phosphonites produced by prior art techniques.
Abstract:
Process for preparing aryl esters of phosphonous acid of formula (V), where A is non-existent or a direct bond or a divalent hydrocarbon bridge with 1 to 6 carbon atoms, which can be substituted by the groups mentioned below, or a heteroatom, cycloalkylidene with 4 to 8 carbon atoms or phenylalkylidene with 7 to 12 carbon atoms, n is equal to 1 or 2, R1 as a monovalent residue denotes certain non-aromatic or aromatic hydrocarbon residues, the aromatic residues denoting substituents such as alkyl, alkoxy, alkylthio, dialkylamino, aryl, aryloxy or halogen, and as a divalent residue denotes a phenylene or naththylene residue, which can carry non-aromatic hydrocarbon residues as substituents, R2 is a non-aromatic hydrocarbon residue with 1 to 18 carbon atoms, aryl, arylmethyl, arylethyl or arylisopropyl, each aryl containing 6 to 10 carbon atoms, and R3 denotes hydrogen or one of the groups mentioned under R2. In a first stage a halogenated hydrocarbon R1(-Hal)¿n?, in which R?1¿ has the above-mentioned meaning, n = 1 or 2, and the halogen has an atomic weight of at least 35, is converted under Grignard conditions with at least molar quantities of magnesium to the corresponding organomagnesium compounds R1(MgHal)¿n?. These are reacted in a second stage with phosphoric acid-bis-arylester halides of formula (VI), where R?2, R3¿ and Hal have the above-mentioned meanings, to form the phosphonous acid arylester (V). The invention also relates to a plastics moulding material, in particular a polyolefin moulding material, containing the phosphonous acid arylester of formula (V). The properties of the moulding material are superior to those of materials which contain phosphonites produced by prior art techniques.
Abstract:
Sweetening agent comprises one or more sweeteners (I) and one or more deoxy sugars (II). Also claimed is the prepn. of the agent are produced by mixing (I) and (II) in powder form, opt. by spray drying an aq. soln. contg. (I) and (II). Pref. (I) is acesulfam K, aspartame, Na cyclamate, saccharin, neohesperidine, dihydrochalcone, trichlorogalacto-sucrose, alitame, thaumatin and stevioside, esp. mixts. of acesulfam K with aspartame or Na cyclamate. (II) is rhamnose or fucose.
Abstract:
Process for preparing aryl esters of phosphonous acid of formula (V), where A is non-existent or a direct bond or a divalent hydrocarbon bridge with 1 to 6 carbon atoms, which can be substituted by the groups mentioned below, or a heteroatom, cycloalkylidene with 4 to 8 carbon atoms or phenylalkylidene with 7 to 12 carbon atoms, n is equal to 1 or 2, R as a monovalent residue denotes certain non-aromatic or aromatic hydrocarbon residues, the aromatic residues denoting substituents such as alkyl, alkoxy, alkylthio, dialkylamino, aryl, aryloxy or halogen, and as a divalent residue denotes a phenylene or naththylene residue, which can carry non-aromatic hydrocarbon residues as substituents, R is a non-aromatic hydrocarbon residue with 1 to 18 carbon atoms, aryl, arylmethyl, arylethyl or arylisopropyl, each aryl containing 6 to 10 carbon atoms, and R denotes hydrogen or one of the groups mentioned under R . In a first stage a halogenated hydrocarbon R (-Hal)n, in which R has the above-mentioned meaning, n = 1 or 2, and the halogen has an atomic weight of at least 35, is converted under Grignard conditions with at least molar quantities of magnesium to the corresponding organomagnesium compounds R (MgHal)n. These are reacted in a second stage with phosphoric acid-bis-arylester halides of formula (VI), where R , R and Hal have the above-mentioned meanings, to form the phosphonous acid arylester (V). The invention also relates to a plastics moulding material, in particular a polyolefin moulding material, containing the phosphonous acid arylester of formula (V). The properties of the moulding material are superior to those of materials which contain phosphonites produced by prior art techniques.
Abstract:
PCT No. PCT/EP91/01158 Sec. 371 Date Dec. 23, 1992 Sec. 102(e) Date Dec. 23, 1992 PCT Filed Jun. 22, 1991 PCT Pub. No. WO92/00306 PCT Pub. Date Jan. 9, 1992.A dibenzo-[c,e] [1,2] oxaphosphorine of the formula I and process of making said compound (I) wherein n=1 or 2 and in which R1 is a monovalent or divalent aromatic radical wherein a Grignard compound R1(MgHal)n is reacted with 6-chloro-6H-dibenzo[c,e][1,2] oxaphosphorine. This compound optionally with phenolic antioxidants, provides stabilization in polymers.
Abstract:
HOE 90/F 201 Novel aryl esters of phosphonous halides and a process for the preparation thereof. Aryl esters of phosphonous halides of the formula I (I) in which R1 is a phenyl or benzyl radical which bears 1 to 3 substituents, methylbenzyl, .alpha...alpha.-dimethylbenzyl, naphthyl or a naphthyl radical bearing 1 to 5 substituents, where the substituents are identical or different and are a non-aromatic hydrocarbon radical, an alkoxy radical or alkylthio radical each having 1 to 8 carbon atoms, aryl or aryloxy each having 6 to 10 carbon atoms or halogen having an atomic number from 9 to 35, R2 is a non-aromatic hydrocarbon radical having 1 to 18 carbon atoms, aryl, arylmethyl, arylethyl or arylisopropyl, where each aryl contains 6 to 1 carbon atoms, R3 is hydrogen or one of the groups mentioned under R2, and X is chlorine or bromine. The invention further relates to a process for the preparation of aryl esters of phosphonous halides of the formula I.