Organic compounds -- part of the class 532-570 series – Organic compounds – Halocarbonate esters
Reexamination Certificate
2002-12-18
2003-09-02
McKane, Joseph K. (Department: 1626)
Organic compounds -- part of the class 532-570 series
Organic compounds
Halocarbonate esters
C558S282000, C562S852000
Reexamination Certificate
active
06613929
ABSTRACT:
The present invention relates to an improved process for the preparation of fluoroformates. It relates in particular to the improved process for the preparation of fluoroformates by exchange of chlorine by fluorine in chloroformates.
STATE OF THE ART
Fluoroformates are known compounds and are very useful as intermediates in the synthesis of organic compounds employed in agriculture or in pharmaceuticals. They make possible particularly the introduction of oxycarbonylated radicals into molecules and advantageously replace chloroformates, which are often unstable under the reaction conditions used.
One of the known processes for the preparation of fluoroformates consists in reacting a carbonyl fluoride halide with an alcohol or a phenol, but this process exhibits several disadvantages. Carbonyl fluoride halides are very difficult to prepare and therefore are very uncommon and very expensive. As they cannot be stored, they have to be manufactured immediately before use. It is also difficult and dangerous to handle them since a special plant is necessary and very low temperatures are used. Furthermore, the sodium fluoride employed must have a specific particle size. The process is consequently not very economical.
Another preparation, described by J. Cuomo and R. A. Olofson (J. Org. Chem., vol. 44, No. 6, 1979), is carried out starting from chloroformates by exchange of the chlorine by fluorine. The reaction is carried out using potassium fluoride in the presence of a catalyst to activate it, such as the crown ether 18-C-6, which complexes the potassium. However, first, crown ethers are not common compounds and they are consequently sold at very high prices; secondly, the reaction times indicated are very high, from 45 hours to 73 hours for aliphatic fluoroformates, 144 hours for aromatic fluoroformates, such as phenyl fluoroformate.
Improvements to this process were then proposed by J. Ichihara et al. (J. Chem. Soc., Chem. Commun., 1986. pp. 793-4). They consist in using a calcined mixture of potassium fluoride and of calcium fluoride in a solvent such as acetonitrile. The reaction time for preparing ethyl fluoroformate is still very high, 24 hours. The calcined mixtures of fluorides have to be carefully prepared beforehand according to a specific procedure and at high temperature.
OBJECTS OF THE INVENTION
It is an object of the invention to obtain fluoroformates from the corresponding chloroformates under better conditions than those of the processes of the prior art and in particular with much shorter reaction times.
This and other objects and advantages of the invention will become obvious from the following detailed description.
THE INVENTION
According to the process of the invention, fluoroformates of the formula
wherein R
1
is a saturated or unsaturated, substituted or unsubstituted and primary or secondary aliphatic, a saturate or unsaturated arid substituted or unsubstituted secondary cycloaliphatic or a substituted or unsubstituted aromatic or heteroaromatic ring, and n is equal to 1, 2 or 3, are prepared by reaction of the corresponding chloroformate of the formula
with an alkali metal fluoride in ethylene carbonate at a temperature wherein the ethylene carbonate is liquid.
The fluoroformates are very rapidly obtained on carrying out the process under these conditions. The reaction time is generally from 1 to 2 hours, both for aliphatic fluoroformates and for aromatic fluoroformates. Their yields and their purities are excellent and often markedly improve with respect to those of the prior art.
The chloroformates which are used as starting compounds are commercially available or are prepared according to the methods known per se.
The process of the invention is preferably carried out by adding the chloroformate to the mixture of the alkali metal fluoride and ethylene carbonate and for best results, this addition is carried out gradually.
The process of the invention is well suited to the preparation of fluoroformates for which the starting chloroformates are stable in highly polar media and are liquid at normal temperatures.
It is also particularly well suited when the fluoroformates which it is desired to obtain are liquid at normal temperature and when they have a markedly lower boiling point than that of ethylene carbonate.
The chloroformates of use are preferably primary and secondary aliphatic chloroformates, non-tertiary cycloaliphatic chloroformates, or aromatic or heteroaromatic chloroformates not carrying strong electron-withdrawing groups on the ring.
R
1
can represent preferably a primary or secondary aliphatic, more preferably a substituted or unsubstituted aliphatic of 2 to 10 carbon atoms, and most preferably, 2 to 8 carbon atoms.
Carbon-carbon double or triple bonds can be present, provided that the double or triple bond is not on the carbon in the 2 position, that is to say that it is not, for example, allyl or propargyl.
The aliphatic chain can be linear or branched and it can comprise heteroatoms, such as oxygen or sulfur atoms. The substituents can be selected in particular from halogenated or nonhalogenated cycloaliphatic or halogenated or nonhalogenated aromatic, provided that the latter are not attached to the carbon carrying the formate group, halogen atoms, provided that they are not attached to the carbon carrying the formate group, or halogenated or nonhalogenated alkoxy or aryloxy.
Mention may be made, as examples, ethyl, n-propyl, isopropyl, vinyl, isopropenyl, n-butyl or isobutyl or derived from the glycol. When R
1
is cycloaliphatic, the latter can be polycyclic. Preferably, the ring attached to the formate group contains 4 to 7 carbon atoms and it can be unsaturated, with the same restrictions as for the aliphatic.
The substituents on the aliphatic ring or rings can be selected from halogen, halogenated or nonhalogenated aliphatic, cycloaliphatic, aromatic, alkoxy or aryloxy. Examples include cycloaliphatic of cyclopentyl, cyclohexyl, adamantyl or cholesteryl.
R
1
can also be a mono- or polycyclic aromatic or heteroaromatic. The ring or rings can carry substituents selected particularly from halogen, halogenated or nonhalogenated aliphatic, cycloaliphatic, aromatic alkoxy or aryloxy, and the like. When the substituents are strong electron-withdrawing, they are generally less suitable.
Heteroaromatic radicals are in particular those in which the hetero ring has 5 or 6 ring members. The heteroatoms of the ring or rings are selected from nitrogen, sulfur or oxygen, preferably from oxygen or sulfur.
Mention may in particular be made, as aromatic, of the substituted or unsubstituted phenyl or naphthyl. As heteroaromatic radical mention may in particular be made of the substituted or unsubstituted furyl, pyrrolyl, thienyl, pyridlyl or pyrimidinyl. As halogen atoms, chlorine, bromine or fluorine are preferably chosen.
One, two or three formate groups can be attached to R
1
. Examples are bisfluoroformate compound, of diethylene glycol bisfluoroformate.
The chlorine-fluorine exchange is carried out using alkali metal fluorides which are commercially available. They are generally used in powder form to accelerate their dissolution in the ethylene carbonate. The alkali metal is preferably sodium or potassium and more particularly potassium.
The amount of alkali metal fluoride with respect to the chloroformate is not critical. According to the stoichiometry of the reaction, it is desirable for at least one fluorine atom per chlorine atom to be replaced to be present in the reaction. Preferably, 1.2 to 2 molar equivalents of alkali metal fluoride with respect to the chloroformate are used.
To obtain the above-mentioned advantages, it is necessary for the reaction to take place in ethylene carbonate which is a compound which is solid at normal temperature. Due to its structure, it might be feared that it will easily decarboxylate or that it will react with the compounds present in the medium.
In point of fact, it has now been found that its use very markedly improves the reaction between the chloroformate and the alkali metal fluoride when it is
Alarcon-Lorca Alphonse
Malfroot Thierry
Senet Jean-Pierre
Isochem
McKane Joseph K.
Muserlian Lucas and Mercanti
Sackey Ebenezer
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