Abstract:
2.2.6.6-Tetramethyl-4-oxopiperidine (I) and its salts were prepd. by reaction of Me2Co with NH3. 340g Me2Co was reacted with NH3 in 64g MeOH contg. 11g NH4Cl as a acid catalyst at 13-17≦̸C for 12hr. 350g MeOH was added to the mixture and heated at 50-55≦̸C for 15-20hr to give 286g I.
Abstract:
Malonates (I; R1 = H, C1-4 alkyl; R2 = C1-12 alkyl, C3-4 alkenyl, Bz, Ph, cyano; R3 = C1-12 alkyl, C3-4 alkenyl, Bz; X = H, C1-12 alkyl, C3-6 alkenyl, C3-4 alkinyl, C2-21 alkoxyalkyl, C7-11 aralkyl, 2,3-epoxypropyl, C1-4 aliph. acyl), useful as a stabilizer for polymer, were prepd. by the reaction of di-lower alkyl-R2,R3-malonate and 4-piperidinol. Thus, 1 g lithium amide, 188.2 g dimethyldiethylmalonate and 320 g 2,2,6,6-tetramethyl-4-hydroxypiperidine were added in 200 ml tigloin, and reacted in N2 gas at 120oC for 6 hr to give bis-(2,2,6,6-tetramethyl-4-piperidinyl)diethylmalonate.
Abstract:
2,2,6,6-Tetramethyl-4-oxopiperidine (I) was prepd. by the reaction of 2,2,4,4,6-pentamethyl-2,3,4,5-tetrahydro pyrimidine (II) with Me2Co, or diaceton alc. 43g IIH2O was reacted with 75g Me2Co and 10 g EtOH at 55≦̸C for 12hr to yield 82% I.
Abstract:
3-ARYL-7-(V-TRIAZOLYL)-COUMARINS IN WHICH THE TRIAZOLYL MOIETY IS OF THE FORMULA
4,5-(-A-)-2H-1,2,3-TRIAZOL-2-YL
AND A REPRESENTS AN OPTIONALLY ALKYL-SUBSTITUTED TETRAMETHYLENE GROUP OR AN OPTIONALLY ALKYL-SUBSTITUTED O,WPHENYLMETHYLENE OR O-W-PHENYLETHYLENE GROUP THE BENZENE RING OF WHICH MAY BE NON-CHROMOGENICALLY SUBSTITUTED, ARE USEFUL AS OPTICAL BRIGHTENERS FOR A GREAT VARIETY OF ORGANIC MATERIALS, E.G. NYLON, POLYETHYLENE GLYCOL TYPE POLYESTER, POLYAMIDE, CELLULOSIC FIBER MATERIALS, AND THE LIKE. A METHOD FOR OPTICALLY BRIGHTENING SUCH ORGANIC MATERIALS, WITH THE AID OF THE NEW COMPOUNDS, AND COMPOSITIONS, ESPECIALLY DETERGENT COMPOSITIONS, CONTAINING THEM HAS OPTICALLY BRIGHTENING INGREDIENTS, ARE ALSO DESCRIBED.
Abstract:
1. A PROCESS FOR THE PRODUCTION OF COUMARINYL-V-TRIAZOLES, COMPRISING (A) ADDING TO 3-PHENYL-7-HYDRAZINO-COUMARIN OF THE FORMULA
2-(O=),3-Y,4-R4,5-R3,6-R2,7-(H2N-NH-)-2H-CHROMENE
OR AN ADDITION SALT THEREOF WITH AN ACID, AN OXIME OF ONE OF THE FORMULAS
V-C(=N-OH)-CO-W AND V-CO-C(=N-OH)-W
THEREBY REACTING THE TWO STARTING COMPOUNDS WITH FORMATION OF THE CORRESPONDING HYDRAZONE OXIME, (B) ADDING THERETO AN OXIDISING AGENT UNDER OXIDISING CONDITIONS IN A SOLVENT STABLE TO OXIDATION, (C) ADDING TO THE RESULTING V-TRIAZOLE OXIDE OF THE CORRESPONDING ONE OF THE FORMULAE
FROM THE REACTION MIXTURE; LIKE SYMBOLS IN THE ABOVE FORMULAE HAVING THE SAME MEANINGS AS FOLLOWS; Y REPRESENTS A PHENYL RADICAL ANY SUBSTITUENT OF WHICH IS SELECTED FROM LOWER ALKOXY, LOWER ALKYL, AND HALOGEN OF AN ATOMIC NUMBER OF AT MOST 35, EACH OF V AND W REPRESENTS, INDEPENDENTLY OF THE OTHER, HYDROGEN, LOWER ALKYL, LOWER ALKYLSULPHONYL, FURYL, A PHENYL RADICAL ANY SUBSTITUENT OF WHICH IS SELECTED FROM HALOGEN OF AN ATOMIC NUMBER OF AT MOST 35, LOWER ALKYL, LOWER ALKOXY, NITRO, CARBOXYL, N,N-DI(LOWER ALKYL)-SULPHAMOYL AND TRIFLUOROMETHYL; OR A PHENYL-LOWER ALKYL RADICAL OR A PHENYL-SULPHONYL RADICAL, ANY SUBSTITUENTS OF THE LATTER TWO RADICALS BEING AT THE BENZENE NUCLEI THEREOF AND BEING SELECTED FROM LOWER ALKYL, LOWER ALKOXY AND HALOGEN OF AN ATOMIC NUMBER OF AT MOST 35; EACH OF R1 AND R4 REPRESENTS HYDROGEN OR LOWER ALKYL, AND EACH OF R2 AND R3 REPRESENTS HYDROGEN, LOWER ALKYL, OR LOWER ALKOXY; OR V AND W TAKEN TOGETHER REPRESENT 4,5-DIHYDRONAPHTHYLENE-(1,2).
Abstract:
LIGHT-STABILIZERS FOR POLYMERIC LIGHT-SENSITIVE PRODUCTS AND MATERIALS ARE PROVIDED WHICH PERTAIN TO THE CLASS OF 2-(2''-HYDROXYPHENYL)-BENZOTRIAZOLES, COMPOSITIONS OF THE COMPOUNDS AND THE LIGHT-SENSITIVE MATERIALS ARE ALSO PROVIDED. IN FURTHER ASPECTS OF THE INVENTION LIGHT-STABLE POLY ADDITION COMPOUNDS ARE PROVIDED WHICH CONTAIN THE 2-(2''HYDROXYPHENYL)-BENZOTRIAZOLE COMPOUNDS AS AN INTEGRAL PART OF THE POLY ADDITION COMPOUNDS. LIGHT-STABLE LINEAR POLYCARBONAMIDES AND LIGHT-STABLE HIGH MOLECULAR WEIGHT POLYESTER MATERIALS ARE ALSO PROVIDED.