US2220638A - Bismuth salts of a substituted malonic acid and process of making them - Google Patents

Bismuth salts of a substituted malonic acid and process of making them Download PDF

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US2220638A
US2220638A US159988A US15998837A US2220638A US 2220638 A US2220638 A US 2220638A US 159988 A US159988 A US 159988A US 15998837 A US15998837 A US 15998837A US 2220638 A US2220638 A US 2220638A
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bismuth
acid
parts
ester
malonic acid
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Boedecker Friedrich
Gruber Heinrich
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/94—Bismuth compounds

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  • This invention relates to the manufacture of oil-soluble, neutral bismuth salts, and it comprises new, normal bismuth salts of substituted malonic acid derivatives having the formula:
  • X represents a substituent of the class consisting of alkoxy and dialkylamide groups, the alkyl substituent in said groups being a lower alkyl radical and R1 and R2 represent lower alkyl groups, said salts having one mol of bismuth combined with 3 mols of said monobasic acid and being neutral, stable compounds of lipoid-like character, soluble in oils and oil solvents; and it further comprises methods of making such normal bismuth salts wherein said monobasic acid derivatives of a substituted malonic acid carrying such branched chain alkyl group are prepared from a corresponding dialkyl ester and the monobasic acids so obtained, or alkali salts thereof, are reacted with a bismuth compound in approximately a molar ratio of 3:1 to produce said neutral, normal bismuth salts; all as more fully hereinafter set forth and as claimed.
  • Stable and permanent bismuth compounds soluble in oils and oil solvents, insoluble in water and having a substantial content of bismuth are a desideratum.
  • normal bismuth salts having a distinctly lipoid character; these normal bismuth salts having 1 mol of bismuth combined with 3 mols of the said substituted monobasic acids.
  • Our new bismuth salts dissolve in solvents for fats e. g. in organic solvents, fatty oils and other liquid fatty acid esters, whereas they are insoluble in water.
  • Monobasic acids formed by amidating one carboxyl of these malonic acids, in lieu of esterifying, give similar results.
  • the new bismuthcompounds are insoluble in water and are of particularly stable character. For therapeutic purposes, this stability is quite important, since their solutions can be readily sterilized by heat.
  • the acids giving these new neutral bismuth compounds are substituted monobasic malonic acids with one carboxyl blocked off with an ester or an amide group and with the methylene carbon of the malonic acid carrying, as a substituent group, a branched chain; a carbon carrying two alkyl groups. They have the general formula, given above; the bismuth carrying three such groups and being a neutral, normal salt of such monobasic acids.
  • R1, R2 and R3 represent a lower alkyl group.
  • R1, R2 and R3 represent a lower alkyl group.
  • the neutral bismuth salts obtained from the above malonic acid derivatives wherein R3 is an alkyl group containing not more than three carbon atoms, such as ethyl or allyl groups, are advantageous.
  • R1 and R2 are methyl, ethyl,propyl,butyl or hexyl groups are also advantageous. All of the above neutral bismuth salts are readily soluble in oil and give stable so:- lutions.
  • the new oil soluble bismuth compounds can be conveniently prepared by causing a reaction between 3 molecules of such an acid, neutralized with an alkali, and 1 molecule of a bismuth salt, such as the nitrate. Reaction is preferably effected in a polyvalent alcohol, such as glycerine or mannitol. It is also possible to make the new compounds by direct neutralization of the free acid with bismuth oxide or hydroxide. But metathetic reaction of an alkali salt with a bismuth salt in a solvent, generally glycerine, is convenient and advantageous. In purifying and recovering the new compounds, advantage can be taken of their solubility in volatile, non-aqueous liquids, such as ether and benzene.
  • Example 1 In a specific embodiment of the present invention, starting with the diethyl-ester of propyl methyl carbin malonic acid (the diethyl-ester of unsymmetrical secondary-amyl' malonic acid) having the formula H5Cr-O J( -OCZHB HvCa-C-OH: i the following procedure may be used to produce a normal bismuth salt having the following formula this salt being a neutral bismuth salt of propylmethyl-carbin-malonic acid monoethyl-ester and containing 25;7 per cent bismuth combined with said monobasic acid.
  • Thesaid diethyl-ester is first converted into the half-ester (monoethyl-ester of secondary amyl-malon'ic acid) by partial saponification to give a monobasic acid of the stated general formula.
  • an alcoholic solution of potash is made, using 56 parts of KOH and 1280 parts of anhydrous or absolute alcohol; both by Weight.
  • 230 parts by Weight of the diethyl ester are slowly added with agitation.
  • the mixture is allowed to stand at the ordinary temperature for a day and the alcohol distilled off, leaving a crystalline residue of the potassium salt of the half-ester. This is dissolved in water and a little unchanged diethyl-ester removed by shaking out the water solution with benzene.
  • This oil represents the neutral bismuth salt or propyl-methyl-carbin-malonic acid monoethyl-ester. It dissolves readily in various non-aqueous organic solvents, in fatty oils and in solvents for fatty oils. It is not soluble in water. It contains 25.7 per cent bismuth (as metal).
  • Example 2 Diethyl-carbin-malonic acid diethyl-ester (the diethyl-ester of symmetrical secondary amylmalonic acid) is half saponified to obtain the corresponding monobasic acid which has the foland which is a colorless oil.
  • Diethyl-carbin-malonic acid half-ester 750 parts by volume of an 8 per cent caustic soda solution are dissolved 303 parts of this diethyl-carbin-malonic acid half-ester.
  • To this solution which is kept cool and vigorously stirred, is added a solution of 242.6 parts by weight of bismuth nitrate in 75 parts by weight of mannit and 500 parts of water. After completion of the addition, stirring is continued for a short time; until the precipitated bismuth salt has completely balled.
  • the aqueous solution is decanted off and the salt dissolved in ether.
  • the ether solution is shaken out with water until the wash water gives no coloration with sodium sulfide.
  • the dried ethereal solution on evaporation of the ether, leaves the neutral bismuth salt of diethyl-carbin-malonic acid halfester as a viscous slightly yellow-colored oil; It is miscible in all proportions with organic solvents and with fatty oils and has the same bismuth content as the product of Example 1, 25.7 per cent.
  • Example 3 Starting with secondary butyl-malonic acid diethyl-ester, 108 parts by Weight are half saponified with 28 parts by weight of caustic potash in 800 parts by volume of alcohol, giving secondary butyl-malonic acid monoethyl ester, a slightly yellow colored oil. Into a cooled solution of 282 parts by weight of this oil in 750 parts by volume of 8 per cent caustic soda solution is introduced a solution of 157.7 parts by weight of bismuth trichloride in a liter of glycerine. Introduction is gradual and stirring vigorous. The further technique is as in Example 1. There is obtained the neutral bismuth salt of secondary butyl-malonic acid ethyl ester, with a bismuth content of 27.1 per cent. In properties, it resembles the products of the previous examples.
  • Example 4 Isopropyl-malonic acid diethyl ester is half saponified with a molecule of KOH in alcoholic solution, as in Example 1. There results isopropyl-malonic acid mono-ethyl-ester as a nearly colorless, quite mobile oil. To 52.2 parts of this oil dissolved in 300 parts by volume of normal caustic soda solution, is added a solution of 48.5 parts by weight of bismuth nitrate in 300 volumes of a 33 per cent glycerine solution. The oily reaction product is treated like that of Example 2. The yield is 68 parts by weight of a viscous oil which is bismuth-isopropyl-malonic acid ethyl-ester with a bismuth content of 28.6 per cent.
  • Example 5 Secondary capryl-malonic acid monoethylester (hexyl-methyl-carbin malonic acid monoethyl-ester) which has the following formula i H502OC OH HsC(CH2)4(
  • Example 6 In the previous examples, a carboxyl of the substituted malonic acid is esterified. The use of an ester group to produce a monobasic acid is, however, not necessary.
  • 230 parts by weight of methyl-propylcarbin-malonic acid diethyl-ester are heated with 110 parts by weight of diethylamine for several hours under pressure to 130 C. From the mixed products of reaction is distilled out as a fraction, the half-ester of methyl-propyl-carbin-malonic- N, N-diethylamido acid (B. B1, ll0-115 0.).
  • the potassium salt obtained by evaporating the alcohol is dissolved in water and by super-saturating with hydrochloric acid, methylpropyl-carbin-malonic-N, N-diethylamido acid is set free as an oil.
  • This oily monobasic acid has the following formula:
  • HC2 (H) EII To 229 parts by weight of this oil dissolved in 1000 parts by volume of normal caustic soda solution is gradually added, with vigorous stirring, a solution of bismuth nitrate in glycerine. This nitrate solution is prepared from 162 parts by weight of crystalline bismuth nitrate, 320 parts of glycerine and 700 parts of water. The bismuth compound separates as an oil. This is dissolved in ether, the ethereal solution repeatedly shaken out with water and dried over sodium sulfate. The ether is distilled ofi finally distilling under reduced pressure.
  • the neutral bismuth salt of methyl-propyl carbin malonic N, N-diethylamido acid is obtained as a thick oil with a yield of 244 parts, by weight.
  • the oily salt dissolves very readily in organic solvents and in fatty oils. Its content of bismuth is 23.4 per cent.
  • a neutral bismuth salt containing 23.4 per cent bismuth is produced as a thick, nearly colorless oil, starting with diethyl-car'bin-malonic acid diethyl-ester and diethyl-carbin-malonic-N, N-diethyl-amido acid monomethyl-ester (liquid HsCa B. P.1-109-l13 G.) and diethyl-carbin-malonic- N, N-diethyl-amido acid prepared therefrom, by.
  • a neutral bismuth salt is obtained in the same Way from the ethyl ester of secondary butylmalonic-N, N-diethyl-amido acid (B. P11, 145- 148 C.) with the aid of amido acid. It is a viscous oil with a bismuth content of 25.1 per cent.
  • the old carbin terminolo y is used; one carbon atom being regarded as methane (carbin) and the substance described as a substituted methane.
  • dialkyl esters of the substituted malonic acids are convenient points of departure in practicing the present invention and in the examples given they are used as source materials. With one equivalent of alkali they can be half saponified to alkali salts of monobasic acids or half-esters which are brought into reaction with ordinary bismuth salts in a 3:1 molecular ratio. Amidated derivatives prepared from dialkyl esters are used in the same way.
  • the alkyl group in the dialkyl ester and in the half-ester is generally ethyl but methyl and propyl compounds are also useful, giving final bismuth compounds of somewhat different character. For some purposes the difference is advantageous.
  • X represents a substituent of the class consisting of alkoxy and dialkylamide groups, the alkyl substituent in said groups being a lower alkyl radical, and R1 and R2 represent a lower.
  • X represents a substituent of the class consisting of alkoxy and dialkylamide groups, the alkyl substituent in said groups being a lower alkyl radical, and R1 and R2 represent a lower alkyl group.

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US159988A 1936-08-26 1937-08-19 Bismuth salts of a substituted malonic acid and process of making them Expired - Lifetime US2220638A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1062692B (de) * 1955-07-05 1959-08-06 Dr Hans Erlenmeyer Verfahren zur Herstellung von entzuendungshemmend wirkenden 4-Hydroxy-isophthalsaeuremonoamiden
DE1109664B (de) * 1954-06-28 1961-06-29 California Research Corp Verfahren zur Herstellung von Metallsalzen von N-substituierten Terephthalamidsaeuren
US4048527A (en) * 1973-09-28 1977-09-13 Skf Industrial Trading And Development Company, B.V. Stator aggregate for rotating electric machines
US5021598A (en) * 1989-07-24 1991-06-04 Mooney Chemicals, Inc. Process for making bismuth carboxylates

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1109664B (de) * 1954-06-28 1961-06-29 California Research Corp Verfahren zur Herstellung von Metallsalzen von N-substituierten Terephthalamidsaeuren
DE1062692B (de) * 1955-07-05 1959-08-06 Dr Hans Erlenmeyer Verfahren zur Herstellung von entzuendungshemmend wirkenden 4-Hydroxy-isophthalsaeuremonoamiden
US4048527A (en) * 1973-09-28 1977-09-13 Skf Industrial Trading And Development Company, B.V. Stator aggregate for rotating electric machines
US5021598A (en) * 1989-07-24 1991-06-04 Mooney Chemicals, Inc. Process for making bismuth carboxylates

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CH201761A (de) 1938-12-15
FR825896A (fr) 1938-03-16

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