Classifications

• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J19/18—Stationary reactors having moving elements inside
  • B01J19/22—Stationary reactors having moving elements inside in the form of endless belts
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
  • B01J19/06—Solidifying liquids
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C231/00—Preparation of carboxylic acid amides
  • C07C231/02—Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines

Definitions

• the invention relates to a process for the preparation of solidified organic compounds, in particular carboxylic acid amides, the carboxylic acid residue of which is substituted by at least 1 fluorine atom.
• Perfluorocarboxamides are intermediates in chemical synthesis.
• Trifluoroacetamide can be used, for example, as a reagent for the production of primary amines from halides or mesylates.
• N-methyltrifluoroacetamide is an intermediate for the production of N-silylated derivatives. It is also useful as a reagent for the preparation of secondary N-methylalkylamines.
• Other partially fluorinated amides can be converted to corresponding unsaturated amides or nitriles, see U.S. Patent 2,730,543. The compounds produced are then the starting material for the production of polymers and copolymers.
• Corresponding partially fluorinated amines can be obtained by hydrogenating fluorinated amides, including N-substituted or N, N-disubstituted amides.
• a simple method of preparation involves reacting esters of fluorinated carboxylic acids with the corresponding amine. Alcohol is released. The amide precipitates and a simple isolation method involves filtering the precipitated amide and then drying it. Such a method is disadvantageous for (large) technical use because the filters clog and the product is contaminated by trapped alcohol.
• Object of the present invention is to provide a method that overcomes these disadvantages of the prior art.
• Another object of the invention was to provide a device which allows the preparation and isolation of carboxylic acid amides in special and solidified organic compounds in general in a simple manner. This object is achieved by the method and the device of the present invention.
• the invention in the broadest sense relates to a process for the preparation of organic compounds which have a melting point greater than 30 ° C. at ambient pressure and are present as a mixture with organic impurities, the organic impurities having a boiling point of up to 120 ° C., the mixture keeps liquid, heated so that the organic compounds evaporate, the organic compound freed from the evaporated organic impurities is divided into smaller volumes and these are converted into the solid state with cooling, with the proviso that the boiling point of the organic compound is at least 40 ° C is higher than the boiling point of the impurity and that the organic compound is thermally stable up to the boiling point of the organic compound.
• the organic compound is preferably a peptide.
• the peptide in the chain is very particularly preferably substituted by fluorine or has a fluorine-substituted protective group.
• R represents Cl-C4-alkyl which is substituted by at least 1 fluorine atom
• R 1 and R 2 are identical or different and stand for hydrogen or Cl-C4-alkyl or in which
• R 1 and R 2 together with the nitrogen atom form a 5- or 6-ring system and the melting point of the compounds of the formula (I) at normal pressure is at least 40 ° C.
• R has the abovementioned meaning and R 3 represents Cl-C6-alkyl, substituted Cl-C6-alkyl or aryl such as phenyl or benzyl,
• R 1 and R 2 have the meaning given above. It takes place in a reactor, a mixture of carboxamide of the formula (I) and liberated alcohol R 3 OH being formed,
• C1-C4-alkyl is also intended to include substituted C1-C4-alkyl, for example C2-C4-alkyl, which in ⁇ position is substituted by the thiomethacrylate radical, as described in US Pat. No. 3,445,491.
• R preferably represents CF 3 , CF 2 H, CF 2 C1, CF 3 CFH or CF 3 CF 2 .
• R 1 and R 2 are the same or different and are preferably hydrogen, CH 3 , C 2 H 5 or C 3 H 7 . Both R 1 and R 2 are very particularly preferably hydrogen, or R 1 is hydrogen and R 2 is CH 3 , C 2 H 5 or C 3 H 7 .
• R 3 preferably represents CH 3 , C 2 H 5 , C 3 H 7 or CF 3 CH 2 .
• the purpose of dividing the reactor contents into “smaller volumes” is to convert these smaller volumes to the solid state in an acceptable time.
• the size of the "smaller volumes” is chosen so that technically manageable particle sizes are achieved.
• the term “smaller volume” preferably stands for particles with a volume content of 91 to 20 ml. Of course, there is no reason not to produce particles with a larger or even smaller volume content.
• a preferred embodiment provides that the carboxylic acid amide of the formula (I), which is divided into smaller volumes, is applied to a cooled base, for example by spraying or spraying. It is preferably dripped on, in particular with the addition of gravity.
• a particularly preferred cooled underlay is a cooled treadmill (cooling belt). This is preferably an endless belt. Water, for example, can be used as the cooling medium.
• the application of the "smaller volumes" to the treadmill is preferably carried out by means of a rotating perforated roller.
• the liquid carboxylic acid amide is introduced into the roller and drips onto the holes chilled treadmill. The drops solidify and can then be wiped off.
• the alcohol is preferably evaporated off in vacuo.
• Another object of the invention is a device that can be used to carry out the method described above. It comprises a heatable reactor which is connected to a rotatable perforated roller via preferably heatable lines.
• the device further comprises a cooled treadmill, preferably a cooled endless treadmill.
• the perforated roller is preferably arranged in such a way that liquids which have been added can drip onto the cooled treadmill using gravity.
• FIG. 1 shows a simple device.
• the stylized reactor (1) has an agitator. Lines for introducing the reactants and devices for generating a vacuum, measuring devices etc. have been omitted for the sake of simplicity.
• the reactor is connected via a heatable line (2) to a feed container (l 1 ) and this via a heatable line (2 ') to a heatable perforated roller (3).
• the liquid material is placed in drops (drops (6) are indicated) on the endless belt (4) via the rotating perforated roller (3).
• the endless treadmill is moved via drive rollers (5) and (5 1 ). Devices for cooling the treadmill are omitted for the sake of simplicity. For example, it can be sprayed with cold water on the underside.
• the drops (6) solidify on the cooled treadmill (4) and form solid particles (7). These fall from the treadmill at the turning point of the drive roller (5 ') into a container provided. If necessary, a scraper device can also be provided, with which the solid particles (7) are lifted off the treadmill and transferred to a container.
• the invention allows the (large) industrial production of carboxamides in a simple manner. The following examples are intended to illustrate the invention without restricting its scope.
• a 90-liter Pfaudier kettle which can be acted upon by vacuum, with a stirrer, gas inlet and 3 column sections, acts as the reactor, the gas being introduced via an immersion tube and cooler.
• the reactor (Pfaudier boiler) is connected to a storage tank via a heated line.
• the storage container is intended to avoid pressure fluctuations.
• the storage container is connected to a rotating perforated roller (Rotoformer) via another heated line.
• the reaction product which leaves the rotoformer in drops, is placed on a cooling belt.
• the cooling belt consists of a 150 mm wide, continuously welded stainless steel belt mounted on 2 drive rollers with a diameter of 150 mm.
• the rear drive roller is rotated by a motor via a chain drive.
• Nozzles are attached below the cooling belt, which direct the cooling medium directly onto the underside of the cooling belt.
• the belt length is 2.70 m from the feed unit (Rotoformer). At the end of the cooling belt there is a scraper that lifts the particulate solid material off the belt.
• the feed unit ie the rotating perforated roller (Rotoformer) for the liquid-held reaction product, consists of a rotating roller with 15 holes per row, which have a diameter of 1.2 mm and a distance of 8 mm between the individual holes as well as the individual rows. The holes in the individual rows are staggered.
• the Rotoformer is also controlled by a DC motor and chain drive.
• the trifluoroacetic acid ethyl ester (TFAEt) was introduced and methylamine was introduced at room temperature. As a result of the exothermic reaction, the reaction mixture warmed up to 80 ° C. After the reaction had ended, the ethyl alcohol was evaporated in vacuo (20 mbar, start temperature in the bottom 55 ° C.). The contents of the reactor were then cooled to 60 ° C., the reactor was aerated and the reaction mixture was transferred to the storage container via a metering pump. Storage container and perforated roller were tempered to 55 ° C. Water heated to 13 ° C served as the cooling liquid for the treadmill. 13.7 kg of the amide were produced in the form of flakes per hour.
• TFAEt trifluoroacetic acid ethyl ester
• the temperature was raised as the alcohol content decreased.
• the column temperature at the top was between 18 u. 19 ° C, the sump and the first shot were run as warm as possible in order to better remove the ethanol from the system.
• the reflux amount was max. 3 1 / h.
• the amide boiled in vacuo ( ⁇ 20 mbar)
• the melt was boiled briefly to remove the last ethanol residues.
• the contents were cooled to 85 ° C., the system was ventilated and conveyed via the floor drain and metering pump into the storage container of the cooling belt in order to avoid pressure fluctuations (filling via static pressure). All lines were heated.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Peptides Or Proteins (AREA)

Applications Claiming Priority (3)

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• 2002
  • 2002-03-21 DE DE10212526A patent/DE10212526A1/de not_active Withdrawn
• 2003
  • 2003-03-11 EP EP03717205A patent/EP1490329A1/de not_active Withdrawn
  • 2003-03-11 JP JP2003578319A patent/JP2005533006A/ja active Pending
  • 2003-03-11 AU AU2003221495A patent/AU2003221495A1/en not_active Abandoned
  • 2003-03-11 WO PCT/EP2003/002453 patent/WO2003080563A1/de not_active Ceased
• 2004
  • 2004-09-20 US US10/944,418 patent/US20050267290A1/en not_active Abandoned

Non-Patent Citations (1)

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