Abstract:
1. A PROCESS FOR THE CATALYTIC REDUCTION OF 2-OXIMINO-6NITROHEXANAMIDE TO PRODUCE AN ALKANOIC ACID SALT OF D,L-LYSINE AMIDE, COMPRISING: SUBJECTING 2-OXIMINO-6NITROHEXANZMIDE, AN ALKANOIC ACID CONTAINING 1-5 CARBON ATOMS AND HYDROGEN IN THE PRESENCE OF A RHODIUM METAL HYDROGENATION CATALYST, TO SUPERATMOSPHERIC PRESSURE, AT A TEMPERATURE ABOVE 15* C. TO CONVERT THE 2-OXIMINO-6NITROHEXANAMIDE TO SAID ALKANOIC ACID SALT OF D,L-LYSINE AMIDE.
Abstract:
A PROCESS FOR TRANSFORMING AN ALKYL AMINO ACID SALT OF A MINERAL ACID INTO THE CORRESPONDING N-ACYL AMINO ALKANOIC ACID COMPRISING NEUTRALIZING THE MINERAL ACID PORTION. THE AMMONIUM SALT IS SEPARATED OUT BY ADDING ALKADROXIDE, SEPARATING OUT THE THEREBY FORMED AMMONIUM SALT OF THE MINERAL ACID, AND ACYLATING THE REMAINING SOLUTION. THE AMMONIUM SALT IS SEPARATED OUT BY ADDING ALKANOC ACID TO THE NEUTRALIZED SOLUTION.
Abstract:
METHODS FOR THE PURIFICATION OF D,L,-LYSINE AMIDE OR CARBOXYLATE SALTS THEREOF, BY FORMING AN ADDUCT WITH CO2, HCL OR HBR, WHICH SEPARATES OUT AS A SOLID.
Abstract:
2-NITRO-6-OXIMINO CYCLOHEXANONE CAN BE REACTED WITH ANHYDROUS AMMONIA IN A SOLVENT SELECTED FROM THE GROUP CONSISTING OF C1 TO C4 ALKANOLS AND C4 TO C8 ALIPHATIC AND ALICYCLIC MONO- OR DI-ETHERS TO AFFORD 2-OXIMINO-6NITRO-CAPROMIDE, A PRECURSOR OF LYSINE.
Abstract:
1. IN A METHOD FOR THE RACEMIZATION OF OPTICALLY ACTIVE MATERIAL OF THE GROUP CONSISTING OF A-AMINOCAPROLACTAM AND LYSINE AMIDE AND MIXTURES THEREOF BY HEATING IN THE PRESENCE OF A STRONG BASE, THE IMPROVEMENT WHICH COMPRISES EMPLOYING ANHYDROUS AMMONIA AS SOLVENT AND HEATING SAID MATERIAL IN SOLUTION THEREIN AT CONCENTRATION OF AT LEAST 10 PERCENT BY WEIGHT.
Abstract:
2-OXIMINO-6-NITRO HEXANAMIDE IS SUITABLY PURIFIED BY RECRYSTALLIZATION FROM A SOLVENT SELECTED FROM THE GROUP CONSISTING OF (A) C1 to C3 dialkyl ethers of ethylene glycol, and (b) C2 to C5 halogenated alkanes having a Cl/C atom ratio ranging from about 1:1 to 1:3.