公开(公告)号：US3753884A

公开(公告)日：1973-08-21

申请号：US3753884D

申请日：1971-04-15

Applicant: AQUITAINE TOTAL ORGANICO

Inventor： KERN R ,  POULAIN C ,  NAHMIAS A ,  LUCAS G

IPC: B01J19/12 ,  C07C249/06 ,  C07C251/44 ,  B01J1/10

CPC classification number: C07C201/00

Abstract: A PHOTOSYNTHESIS PROCESS IS PROVIDED FOR THE PREPARATION OF HYDROCHLORATES OF CYCLOALKANONE OXIMES CONTAINING MOREE THAN 5 CARBON ATOMS, BY THE REACTION UNDER IRRADIATIOON OF NITROSYL CHLORIDE IN A CYCLOALKANE SOLUTIOON IN WHICH THE NITROSYL CHLORIDE IS PREPARED IN SITU IN ONE SECTION OF THE REACTOR, KNOWN AS THE NON-OXIMATING ZONE, SEPARATED BY A PARTITION WITTH AN OVE

公开(公告)号：US3734845A

公开(公告)日：1973-05-22

申请号：US3734845D

申请日：1971-03-16

Applicant: AQUITAINE TOTAL ORGANICO

Inventor： BRAVI J ,  POULAIN C ,  VIALLET C

IPC: B01J19/12 ,  B01J1/10 ,  C07C3/24

CPC classification number: B01J19/123 ,  Y10S204/903

Abstract: A PROCESS FOR THE CONTINUOUS PREPARATION OF CYCLOALKANONE OXIMES BY THE ACTION OF NITROSYL CHLORIDE PREPARED IN SITU IN A SULPHURIC MEDIUM ON A LIQUID CYCLOALKANE OR A CYCLOALKANE DISSOLVED IN AN ORGANIC SOLUTION WHICH IS INERT UNDER THE REACTION CONDITIONS, UNDER THE EFFECT OF ACTINIC RADIATION, CHARACTERIZED BY THE FACT THAT, FOR A GIVEN CONCENTRATION OF OXIME IN THE SULPHURIC MEDIUM, THE MINIMUM TEMPERATURES OF THE SURFACES TRANSMITTING THE LIGHT ENERGY AND IN CONTACT WITH THE REACTIVE

MIXTURE ARE MADE TO VARY IN INVERSE PROPORTION TO THE PERCENTAGE WEIGHT OF THE SULPHURIC MEDIUM IN THE REACTIVE MIXTURE.

公开(公告)号：US3825532A

公开(公告)日：1974-07-23

申请号：US19232771

申请日：1971-10-26

Applicant: AQUITAINE TOTAL ORGANICO

Inventor： KERN R ,  POULAIN C ,  TOCK F

IPC: C07D201/04 ,  C07D41/00

CPC classification number: C07D201/04

Abstract: A PROCESS FOR REARRANGING CYCLODODECANONEOXIME INTO PURE CYCLODODECALACTAME, CHARACTERIZED BY THE FACT THAT THE OXIME, CONVERTED INTO OXIME CHLORHYDRATE, IS MADE INTO A SOLUTION WITH A SELECTIVE SOLVENT, IN THE PRESENCE OF A SMALL QUANTITY OF CATALYST, CHOSEN FROM THE GROUP OF ACID HALIDES AND OXYHALIDES, AND THEN HEATED TO A TEMPERATURE OF BETWEEN 65 AND 110* C. FOR ONE TO TWO HOURS, THE RESULTING HYDROCHLORIC ACID IS DRAWN OFF BY MEANS OF A FLOW OF GAS WHILE MAINTAINING THE REFLUX TEMPERATURE OF THE SOLVENT, THE REACTION MIXTURE IS WASHED WHILE HOT WITH AN ALKALINE AQUEOUS SOLUTION, THE ORGANIC PHASE CONTAINING THE LACTAME IS WASHED IN HOT WATER UNTIL BECOMES NEUTRAL, AND THE LACTAME IS RECOVERED BY CRYSTALLIZATION OR DISTILLATION OF THE SOLVENT. THE QUANTITY OF CATALYST USED RANGES FROM 0.5 TO 5%, AND PREFERABLY 1 TO 2%, OF THE WEIGHT OF OXIME. THE SOLVENT IS PREFERABLY SELECTED FROM ALKANES, CYCLOALKANES, SUBSTITUTED ALKANE AND CYCLOALKANE DERIVATIVES, AND HALOGENATED ALKANE AND CYCLOALKANE DERIVATIVES.