Classifications

• • 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

• This disclosure relates to the methods for the production of carboxylic amides. Specifically, this disclosure relates to a method wherein a carboxylic acid is reacted with near-stoichiometric amounts of an amine having a boiling point below about 150°C.
• GB 2,160,421 discloses a method for preparing stearamidopropyl dimethylamine by reacting 270 parts stearic acid with 100 parts dimethyiamino propyi amine, under pressure, at a temperature of 140°C to 150°C for three hours. The reaction temperature is then increased to 165°C to 170°C and held for one hour completing the reaction. Expensive separation apparatus is suggested when high yields are desirable.
• JP 3060957-A discloses the preparation of fatty acid bisamides by reacting fatty acid with a diamine at a molar ratio of 1.85-2.1 :1 wherein the reaction temperature is 150-300°C.
• the reaction is initially conducted under pressure (7-30kg/cm2) and when the conversion to fatty acid bisamide reaches 85- 95wt% based on the diamine, the reaction system is returned to normal pressure.
• JP 6 279 375-A discloses a method for the preparation of carboxylic acid amides that uses pressure but also uses expensive separation equipment for water removal and also uses large excesses of amine. It would be desirable to produce carboxylic amides without the need for expensive recovery equipment, while removing the necessity of releasing excess amine into the environment.
• the method for producing carboxylic amides described herein involves combining near-stoichiometric amounts of carboxylic acid and amine in a reaction vessel and reacting under pressures greater than atmospheric pressure.
• reaction of carboxylic acid and amine is conducted at atmospheric pressure using a large excess of amine.
• a bleaching agent is optionally included in the reaction mixture of either embodiment in order to improve the color of the final product.
• R C II OH wherein R is an aliphatic or aromatic group, preferably a saturated or unsaturated aliphatic group having from 5 to 24 carbon atoms.
• R is a linear or branched alkyl or alkylene group.
• R can also be an organic group containing a hetero atom, provided the hetero atom does not interfere with the reaction with the amine.
• the R group is selected from the group consisting of C7-C21 branched or linear, saturated or unsaturated alkyl groups.
• Particularly useful acids include vegetable and animal based fatty acids, including, but not limited to decanoic acid, lauric acid, myristic acid, palmitic acid, stearic acid, oleic acid, erucic acid, behenic acid, coconut acid and tallow acid.
• Any primary or secondary amine having a boiling point below about 200°C, preferably below about 160°C can be employed in the method of the present invention.
• Preferred amines are of the formula:
• R1 is hydrogen, alkyl or alkenyl
• R2 is a bridging group having up to 8 carbon atoms and which may be optionally substituted with hetero atoms or carbonyl groups or combinations thereof
• R3 and R4 can be the same or different and are individually selected from the group consisting of hydrogen and C1-C6 alkyl.
• a particularly useful amine is 3-dimethylamino propylamine ("DMAPA").
• DMAPA 3-dimethylamino propylamine
• the molar ratio of amine to carboxylic acid will be in the range of 0.8:1 to 1.2:1.
• no more than about 1.1 moles of amine is present for each mole of acid groups present in the reaction mixture.
• the reactants are added to a reaction vessel in a nitrogen atmosphere and reacted at temperatures in the range of about 40°C to about 210°C at pressures ranging from about 0 psi to about 125 psi, preferably about 90 psi to about 105 psi. Overall reaction times are from about 10 hours to about 24 hours.
• the pressure within the reaction vessel will increase due to the formation of water.
• the reaction vessel is vented to maintain a pressure below about 105 psig.
• the endpoint in the reaction can be determined by measurement of the residual fatty acid.
• an excess of amine is used in the reaction mixture and the reaction of carboxylic acid and amine is carried out at about atmospheric pressure.
• the reaction is carried out at temperatures in the range of from about 80°C to about 200°C. Reaction times can range from about 8 to about 30 hours, preferably from about 12 to about 24 hours.
• a bleaching agent can be employed during the reaction. Suitable bleaching agents include hypophosphorous acid. When used, bleaching agent should be added in an amount from about 100 to about 4000 ppm by weight based on the combined amount of the acid and amine, preferably from about 500 to about 3000 ppm. In this embodiment, an excess of amine is employed. It is preferred that about 5 to about 50 percent excess amine is employed.
• amine e.g., Dimethylaminopropylamine or N,N Dimethylpropane diamine
• carboxylic acid is a condensation reaction, and proceeds with the elimination of water.
• Water is preferably constantly removed from the reaction zone to allow the reaction to proceed to completion, and achieve a low residual acid content.
• a nitrogen sparge can be used to assist water removal.
• hypophosphorus acid is optionally used during the reaction to bleach the product and assure a light colored product is made.
• the reaction is run at atmospheric pressure with an excess of amine.
• unreacted amine is stripped from the reaction mix by applying vacuum to the system.
• the quantity of excess amine required significantly depends on the effectiveness of the overhead reflux system associated with the reactor. Nominally 25%-35% excess amine will be required on a commercial scale.
• Excess amine is constantly removed from the reaction mass along with the evolved water.
• an overhead "hot" reflux system should separate the water/amine mixture, returning the amine to the reactor, while allowing the water to exit the system to a cold condenser for recovery in a distillate receiver tank.
• the reactor is preferably heated quickly to 130°C, and then put into a slow heat-up vs. time ramp mode. At about 140°C the reaction proceeds rapidly. The temperature is held at this point for approximately two hours before additional ramping further accelerates the reaction rate. The temperature is ramped very slowly, (e.g. 5°C/30 min.), from 140°C to 180°C to prevent requiring a higher excess amine level than noted above. A second holding period occurs at 180°C. The reaction phase is over when the residual acid falls below 3%. Then excess amine stripping is initiated. The distillate from the reaction and amine stripping phases contains all of the excess amine and water generated by the reaction.
• the amine can advantageously be recycled back to the reactor for economic and environmental purposes.
• Amine recycle is accomplished by adding the amine/water condensate to the full charge of acid. By the addition of the water/amine mixture to the acid, it is postulated that an amine salt forms which reduces the vapor pressure of the amine to a level where water can be selectively removed.
• the water (from the prior reaction) is then stripped out by heating the batch to about 150°C. Amine losses from this step are below 0.15% of the total recycle and fresh amine charges (typically the losses are below 0.05% of the fresh and recycle amine charges).
• the batch is then cooled to 70°C, and a stoichiometric charge of fresh amine is added for the next reaction.
• the fresh amine charge also accounts for minor amine losses though processing inefficiencies (e.g., low level vent losses or other handling losses).
• an odor stabilizer optionally can be added to the product.
• the present fatty acid amides when freshly made have a mild, but not unpleasant odor.
• amides derived from fully saturated fatty acids the possibility of oxidative instability would be considered unlikely by those skilled in the art, and the formation of pyridines not predicted. It is a surprising discovery, therefore, that during storage, these products developed an undesirable "pyridine" like odor. Analysis of product having this characteristic odor revealed the presence of low levels of volatile pyridine derivatives.
• an odor stabilizer can be present in an amount from about 50 ppm to about 5000 ppm, preferably about 500 ppm to about 1500 ppm.
• antioxidants useful in the context of the present invention include, but are not limited to phenolic antioxidants such as: 3,5-Di-tert-butyl-4-hydroxy toluene (BHT); 3,5-Di-tert-butyl-4-hydroxy anisole (BHA); Corn oil-60%, butylated hydroxytoluene-20%, butylated hydroxyanisole-10%, propyl gallate-6%, citric acid-6%; Octadecyl 3-(3,5-di-tert-butyl-4-hydroxy-phenyl)propionate; and 3,5- Di-tert-butyl-4-hydroxyhydrocinnamic acid, triester with 1 ,3,5-tris(2- hydroxyethyl)-s-triazine-2,4,6(1 H,3H,5H)-trione.
• BHT 3,5-Di-tert-butyl-4-hydroxy toluene
• BHA 3,5-Di-tert-butyl-4-hydroxy
• Suitable antioxidants include those available under the tradenames. IRGANOX® 1076 and IRGANOX® 3125 from Ciba Geigy Corporation, and under the tradenames TENOX®4 and TENOX®6 from Eastman Chemical Co.
• Other antioxidants useful herein are readily apparent to one of ordinary skill in the art and can be found, for example, in McCutchen's Functional Materials, 1995 McPublishing Co., N.J., U.S.A., the relevant portions thereof being incorporated herein by reference.
• butylated hydroxytoluene (BHT) is employed as a odor stabilizer in an amount of between about 500 and 1500 ppm.
• BHT butylated hydroxytoluene
• the resulting carboxylic amides are useful as surfactants.
• the following non-limiting examples illustrate procedures useful in practicing the methods described herein.
• Decanoic acid (670 g) is added to an autoclave and the system is purged with nitrogen.
• Dimethylaminopropylamine (403 g) is added to a bomb and the bomb is purged with nitrogen.
• the DMAPA is added to the autoclave by means of nitrogen pressure. The excess pressure in the autoclave is vented and the batch temperature is increased to 175°C with the autoclave sealed. After 4 hours the decanoic acid content drops to 4-5% and the pressure (approx 80psi) from the water formed during the reaction is vented gradually over a 45 minute period.
• the autoclave is then sealed and the temperature is increased to 205°C and held for 1-2 hours after which the residual pressure is vented once again. With the aid of a slow nitrogen sparge the reaction is then completed (decanoic acid ⁇ 2%) at 205°C and atmospheric pressure.
• Decanoic acid 125 lbs
• hypophophorous acid 85 gms
• the acid is heated to 80°C at atmospheric pressure.
• DMAPA is blown into the autoclave using nitrogen gas.
• DMAPA is added at a rate of 1 Ib./min to avoid excessive heat build up from the resulting exothermic reaction.
• a total of 76 lbs DMAPA is added.
• Temperature is adjusted to be in the range of 95-110° during DMAPA addition. The temperature is raised to 180°C and held for four hours. Pressure within the autoclave increases during this period due to the formation of water. The autoclave is vented as necessary to maintain pressure at about 75 psig.
• the mixture is sampled and tested for residual acid using techniques known to those skilled in the art.
• the autoclave is slowly vented to atmospheric pressure.
• the temperature is then increased to about 200°C and reaction is continued until sampling shows that the residual acid is less than about 0.15 meq/gm.
• the autoclave is then vented again and reaction continues at 205°C until free acid drops to below about 0.1 meq/gm.
• Example 3 Into a reaction vessel fitted with thermometer, stirrer, vigreux and distillation column was placed 603.0 grams (3.47 moles) of decanoic acid and 1.08 grams of 50% solution hypophosphorous acid. This was stirred and heated to 50°C under nitrogen. 427.5 grams (4.16 moles) of dimethylaminopropylamine was added over a period of 10 minutes. The reaction mixture was heated up to 130°C at a rate of 1 °C per minute. Temperature was raised to 140°C with a ramp rate of 10°C per hour and kept at this temperature for about 2 hours. Then, the temperature was raised to 180°C and held there for one hour. Water and excess amine were stripped off under 29" Hg for 30 minutes, and the distillate collected for recycling.
• the odor stabilizing effect of six different antioxidants is evaluated in this Example.
• the antioxidants evaluated are BHT, TENOX® 4, IRGANOX®1076, BHA, TENOX®6 and IRGANOX®3125.
• a control sample containing no antioxidant is also evaluated. Two samples of each experiment, one stored under a nitrogen atmosphere and one stored in air, are prepared and evaluated.
• Example 3 The procedure for the sample preparation for this Example is as follows. A freshly prepared sample of the carboxylic amide of Example 3 and the antioxidant (1000 ppm by weight) are weighed into a 30 ml of Wheaton glass serum bottle. The mixture is stirred at room temperature by a magnetic stirred for 10 minutes to obtain a homogeneous solution. The bottle is then sealed by a Teflon-lined rubber septum in the presence of either air or nitrogen. Samples being stored under nitrogen are purged once by nitrogen for another 10 minutes to exclude the air. These samples are then subjected to oven aging at 37°C for 36 days. Samples are stabilized at 25°C for 60 minutes before olfactory evaluation.
• control samples (containing no antioxidant) exhibited a strong order whether stored in air or under nitrogen. Each of the antioxidants tested reduced the odor of the carboxylic amide significantly. The samples stored under nitrogen generally exhibited less odor than the corresponding samples stored in air. BHT and TENOX®4 provided the most reduction in odor. While all samples showed some yellowing with time, the samples least affected were those containing BHT and IRGANOX®1076.

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• 1997
  • 1997-04-22 US US08/837,844 patent/US6107498A/en not_active Expired - Lifetime
• 1998
  • 1998-03-19 EP EP98924081A patent/EP0977727B1/en not_active Expired - Lifetime
  • 1998-03-19 EP EP02076778A patent/EP1236710B1/en not_active Expired - Lifetime
  • 1998-03-19 DE DE69815098T patent/DE69815098T2/de not_active Expired - Lifetime
  • 1998-03-19 CA CA002287504A patent/CA2287504A1/en not_active Abandoned
  • 1998-03-19 WO PCT/EP1998/001781 patent/WO1998047860A1/en not_active Ceased
  • 1998-03-19 JP JP54490298A patent/JP2001520664A/ja not_active Withdrawn
  • 1998-03-19 DE DE69835041T patent/DE69835041T2/de not_active Expired - Lifetime
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