USRE23405E - Niteo - Google Patents
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- USRE23405E USRE23405E US23405DE USRE23405E US RE23405 E USRE23405 E US RE23405E US 23405D E US23405D E US 23405DE US RE23405 E USRE23405 E US RE23405E
- Authority
- US
- United States
- Prior art keywords
- nitro
- thenoyl
- chloride
- acid
- thiophene
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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- 238000006243 chemical reaction Methods 0.000 description 28
- XHXFXVLFKHQFAL-UHFFFAOYSA-N Phosphoryl chloride Chemical compound ClP(Cl)(Cl)=O XHXFXVLFKHQFAL-UHFFFAOYSA-N 0.000 description 25
- 239000002253 acid Substances 0.000 description 24
- YTPLMLYBLZKORZ-UHFFFAOYSA-N thiophene Chemical group C=1C=CSC=1 YTPLMLYBLZKORZ-UHFFFAOYSA-N 0.000 description 23
- HPGGPRDJHPYFRM-UHFFFAOYSA-J Tin(IV) chloride Chemical compound Cl[Sn](Cl)(Cl)Cl HPGGPRDJHPYFRM-UHFFFAOYSA-J 0.000 description 16
- UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- 238000000034 method Methods 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 11
- 239000000047 product Substances 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N HCl Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 238000007792 addition Methods 0.000 description 10
- 150000002148 esters Chemical class 0.000 description 10
- 238000009833 condensation Methods 0.000 description 8
- 230000005494 condensation Effects 0.000 description 8
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-Dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 7
- 239000005711 Benzoic acid Substances 0.000 description 7
- 239000000543 intermediate Substances 0.000 description 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 238000006460 hydrolysis reaction Methods 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 5
- -1 nitrobenzoic acid ester Chemical class 0.000 description 5
- ATJFFYVFTNAWJD-UHFFFAOYSA-N tin hydride Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- MVPPADPHJFYWMZ-UHFFFAOYSA-N Chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
- UHZYTMXLRWXGPK-UHFFFAOYSA-N Phosphorus pentachloride Chemical compound ClP(Cl)(Cl)(Cl)Cl UHZYTMXLRWXGPK-UHFFFAOYSA-N 0.000 description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- 239000012442 inert solvent Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 4
- 150000004702 methyl esters Chemical class 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N n-butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 235000014786 phosphorus Nutrition 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- TUCRZHGAIRVWTI-UHFFFAOYSA-N 2-bromothiophene Chemical compound BrC1=CC=CS1 TUCRZHGAIRVWTI-UHFFFAOYSA-N 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 150000001805 chlorine compounds Chemical class 0.000 description 3
- 239000012043 crude product Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- OAICVXFJPJFONN-UHFFFAOYSA-N phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011574 phosphorus Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- UTEQVEMDYYOJGM-UHFFFAOYSA-N 2-(methoxycarbonyl)-3-nitrobenzoic acid Chemical compound COC(=O)C1=C(C(O)=O)C=CC=C1[N+]([O-])=O UTEQVEMDYYOJGM-UHFFFAOYSA-N 0.000 description 2
- PASDCCFISLVPSO-UHFFFAOYSA-N Benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 2
- MLUXSFHNWQBQFJ-UHFFFAOYSA-N COC(C1=C(C(=CC=C1)[N+](=O)[O-])C(C1=CC=CS1)=O)=O Chemical compound COC(C1=C(C(=CC=C1)[N+](=O)[O-])C(C1=CC=CS1)=O)=O MLUXSFHNWQBQFJ-UHFFFAOYSA-N 0.000 description 2
- 102100012409 COCH Human genes 0.000 description 2
- 101700074891 COCH Proteins 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N Carbon tetrachloride Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 229920002301 Cellulose acetate Polymers 0.000 description 2
- RCJVRSBWZCNNQT-UHFFFAOYSA-N Dichlorine monoxide Chemical compound ClOCl RCJVRSBWZCNNQT-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M NaHCO3 Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- LQNUZADURLCDLV-UHFFFAOYSA-N Nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 2
- FYSNRJHAOHDILO-UHFFFAOYSA-N Thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- 230000000875 corresponding Effects 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 238000005755 formation reaction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 2
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- QCUHIFBZUSEOIS-UHFFFAOYSA-N methyl 2-carbonochloridoyl-6-nitrobenzoate Chemical compound COC(=O)C1=C(C(Cl)=O)C=CC=C1[N+]([O-])=O QCUHIFBZUSEOIS-UHFFFAOYSA-N 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 150000003577 thiophenes Chemical class 0.000 description 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-Tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 1
- GSFNQBFZFXUTBN-UHFFFAOYSA-N 2-chlorothiophene Chemical compound ClC1=CC=CS1 GSFNQBFZFXUTBN-UHFFFAOYSA-N 0.000 description 1
- CEEJSCAKNYSVHF-UHFFFAOYSA-N 2-methoxycarbonyl-5-nitrobenzoic acid Chemical compound COC(=O)C1=CC=C([N+]([O-])=O)C=C1C(O)=O CEEJSCAKNYSVHF-UHFFFAOYSA-N 0.000 description 1
- BYFXOXFIQMTBIP-UHFFFAOYSA-N 3-nitro-2-(thiophene-2-carbonyl)benzoic acid Chemical compound OC(=O)C1=CC=CC([N+]([O-])=O)=C1C(=O)C1=CC=CS1 BYFXOXFIQMTBIP-UHFFFAOYSA-N 0.000 description 1
- WETWJCDKMRHUPV-UHFFFAOYSA-N Acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 1
- MPPWGCLUGXDRMX-UHFFFAOYSA-N C(=O)(OC)C1=C(CCl)C=C(C=C1)[N+](=O)[O-] Chemical compound C(=O)(OC)C1=C(CCl)C=C(C=C1)[N+](=O)[O-] MPPWGCLUGXDRMX-UHFFFAOYSA-N 0.000 description 1
- GVGLGOZIDCSQPN-PVHGPHFFSA-N Heroin Chemical compound O([C@H]1[C@H](C=C[C@H]23)OC(C)=O)C4=C5[C@@]12CCN(C)[C@@H]3CC5=CC=C4OC(C)=O GVGLGOZIDCSQPN-PVHGPHFFSA-N 0.000 description 1
- QPJVMBTYPHYUOC-UHFFFAOYSA-N Methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 1
- 210000004940 Nucleus Anatomy 0.000 description 1
- 108060006335 Poc1 Proteins 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 210000002268 Wool Anatomy 0.000 description 1
- 239000012346 acetyl chloride Substances 0.000 description 1
- 150000001266 acyl halides Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000004429 atoms Chemical group 0.000 description 1
- 235000020127 ayran Nutrition 0.000 description 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atoms Chemical group C* 0.000 description 1
- 239000012320 chlorinating reagent Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000005712 crystallization Effects 0.000 description 1
- 230000003247 decreasing Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000295 fuel oil Substances 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- JZBJZIIBESQMQP-UHFFFAOYSA-N methyl 3-carbonochloridoyl-2-nitrobenzoate Chemical compound COC(=O)C1=CC=CC(C(Cl)=O)=C1[N+]([O-])=O JZBJZIIBESQMQP-UHFFFAOYSA-N 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 150000005338 nitrobenzoic acids Chemical class 0.000 description 1
- 125000006502 nitrobenzyl group Chemical group 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- DWYFUJJWTRPARQ-UHFFFAOYSA-N phenyl(thiophen-2-yl)methanone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CS1 DWYFUJJWTRPARQ-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000011528 polyamide (building material) Substances 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propanol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- DNIAPMSPPWPWGF-UHFFFAOYSA-N propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000001256 steam distillation Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
Definitions
- the positions 3- and 5- and in which the alkoxy group contains from 1 to 4 carbon atoms with from 1.0 to 1.5 mols of a thiophene, compound of the class consisting of thiophene, 2-chlorothiophehe and 2-bromothiophene, in an inert organic solvent in the presence of 0.55 to 1.1 mol of anhydrous stannic chloride and at least 1 mol of phosphorus oxychloride, per mol of carboalkoxy-nitrobenzoyl chloride employed, the reaction being carried out at temperatures of from 0 to 20 C.
Description
Reissued Sept. 4, 1951 23,405 NITRO- (2'-THENOYL) -ALKYL BENZOATES Edward K.
E. I. du Pont Gladding, Greenville, DeL, assignor to de Nemours & Company, Wilmington, Del., a corporation of Delaware No Drawing. Original No.
gust 15, 1950, Serial No.
for reissue February 9, 1951,
1949. Application Serial No. 210,278
2,519,040, dated Au- 71,203, January 15.
8 Claims. (Cl. 260-3323) Matter enclosed in heavy brackets I: II appears reissue specification; matter printed in italics indicates the additions made by reissue.
This invention relates to the preparation 01 new substituted 2-(2'-thenoyl) -benzoic acid alkyl esters and the free acids obtainable therefrom, and more particularly to an improved process for the preparation of nitro-2-(2'-thenoyl)-benzoic acid alkyl esters, which may carry chlorine or bromine in the 5'-position of the thiophene nucleus. The new compounds of this invention have the formula:
wherein X=H, C1 or Br, and
R=an alkyl group containing atoms.
The remaining substitutable positions of the benzene and thiophene rings are understood to be occupied by hydrogen.
The literature describes methods by means of which simple acyl halides, such as acetyl chloride and benzoyl chloride, can be condensed with thiophene in the presence of anhydrous stannic chloride as catalyst to produce high yields 0! the respective ketones. According to G. Stadnikov and I. Goldfarb [Ben 61B, 2341-42 (1928) l, the dropwise addition of [anyhydrous] anhydrous stannic chloride to a solution of benzoyl chloride and thiophene in benzene as solvent leads to the production of 2-benzoylthiophene in yields of 82.5% of theory. These authors observed that an oily, insoluble, tin-containing intermediate was formed during the course of the reaction. Similar experiments have been described, and similar results obtained, by G.
from 1 to 4 carbon in the original patent but forms no part of this Stadnikov and V. Rakovski (Chem. Abs. 22, 1774) and Y. Goldfarb (Chem. Abs. 25, 2719), among others.
With various substituted acid chlorides, the process of G. Stadnikov and I. Goldfarb described above gives very poor yields of very poor quality products. For example, the dropwise addition of anhydrous stannic chloride to a benzene solution of 2-carbomethoxy-B-nitrobenzoyl chloride and thiophene gave inconsistent yields of from 32% to 43% of the theoretical of [6-nitro-2- (2'- thenoyl) -benzoic] 3-m'tro-2-(2'- thermal)- benzoic acid methyl ester (as determined by hydrolysis of the crude product to the free acid) and the methyl ester, as obtained, was always badly contaminated with dark colored tarry polymeric materials. Furthermore, during the course of the reaction a tin-containing intermediate separated from the reaction mass in the form of a thick, heavy, black tar which solidified on the walls of the reaction vessel and which could be removed only with great difficulty, which makes the process totally inoperable on a technical scale.
Some improvement in yield and quality of product can be realized [my] by modifying the reaction conditions. Thus, by interchanging the order of addition of anhydrous stannic chloride and thiophene in the process or Stadnikov and Goldiarb, the yield of [6-nitro-2-(2'-thenoyl)- benzoic] 3-m'tr0-2-(2'- thenOyU- benzoic acid methyl ester (as determined by hydrolysis of the crude product to the free acid) obtained by condensing 2-carbomethoxy-3-nitrobenzoyl chloride with thiophene was increased from 32% to 43% of the theoretical to 68%. The ester, however, was contaminated with dark colored, tarry, polymeric materials and an insoluble tin-containing intermediate separated from the reaction mass as the condensation progressed.
It is an object of this invention to prepare nitro-2-(2'-thenoyl)-benzoic acid alkyl esters, which may carry halogen as a substituent in the 5'-position oi the thiophene nucleus. A further objective of this invention is to provide an improved manufacturing process for the production of these new compounds, which is economically feasible and which produces them in high yield and of good quality.
The new compounds of the present invention For example, the alkyl esters may be,
and reduced, or, alternatively, reduced and ringclosed to or 6-]aminothiophanthraquinones carrying, as substituents in the 2-position of the thiophanthraquinone nucleus, hydrogen, chlorine or bromine. These thiophanthraquinone compounds are, in themselves, dyes for cellulose acetate and they may be reacted upon further to produce dyes for cellulose acetate, wool, synthetic polyamide fibers and cellulosic fibers.
The present invention involves the condensation of 2-carboalkoxy-(3 or 5) -nitrobenzoyl chloride with thiophene (or 2-chloroor 2-bromothiophene) in the presence of stannic chloride as catalyst and with a molar equivalent or more of phosphorus oxychloride present in the reaction system.
I have found that, where the condensation of the nitrobenzoic acid ester with thiophene is carried out in a similar manner to that described by Stadnikov and Goldfarb but with the addition of a molar equivalent of phosphorus oxychloride prior to the addition of the anhydrous stannic chloride, at materially increased yield of the nitro-2-(2-thenoyl) -benzoic acid alkyl ester is obtained, and that no tin-containing complex separates out during the process, the reaction mass remaining homogeneous throughout the course of the condensation. A still further increase in the yield and purity of the resulting product is obtained by changing the order of addition of the anhydrous stannic chloride and thiophene, as pointed out above, when at least a molecular equivalent of phosphorus oxychloride introduced into the reaction mass prior to the thiophene. Under these conditions, a yield of from 83% to 86% of the theoretical of [Ci-nitro- 2-(2-thenoyl) -benzoic] 3-nitro-2- (2-thenoyl) benzoic acid methyl ester is obtainable. The crude ester is crystalline, light in color, and contains only small amounts of polymeric impurities. Again the reaction mass remains homogeneous throughout the course ofv the condensation.
The exact operation 01 the phosphoru oxychloride in the reaction is not understood. It is possible that the. mixture oiphosphorus oxychloride and benzene is a more powerful solvent for the tin-containing intermediate than benzene alone and thus holds the intermediate in solution, although it appears more likely that the anhydrous stannic chloride and phosphorus oxychloride form a molecular addition compound which serves to catalyze the reaction but which does not combine with the product to form an insoluble intermediate.
The following examples are given to illustrate the invention. The parts used are by weight, unless otherwise designated.
Example 1 One (1.00) part of 2-carbomethoxy-3nitrobenzoic acid suspended and agitated in 1.96 parts of benzene was treated at room temperature with 1.02 parts of phosphorus pentachloride to convert the acid to the acid chloride. A vigorous reaction set in as soon as the phosphorus pentachloride was added and much hydrogen chloride was evolved. The reaction was completed by heating the charge to 60-65 C. for 5 to 10 min-- utes. Formation of the acid chloride took place according to the following equation:
o on PC], -o COCHs om 5 POC1| H01] P -C] s P0013 I I ShOh I 0-00m 'COCH; 02N 02N A Anhydrous stannic chloride and phosphorus oxychloride were destroyed by treating the reaction mass with a solution of 0.524 part of concentrated hydrochloric acid in 2.22 parts of water.
Upon steam-distilling the mass free of benzene, [6 nitro 2 2-thenoyl) benzoic] 3-nitm-2- (2'-thenoyl) -benzoic acid methyl ester separated as a heavy oil which crystallized quickly to a tan colored solid and which was separated by filtration, slurried in a dilute solution of sodium bicarbonate, filtered, washed with water and dried. The yield was 1.11 parts, equal to 86% of the theoretical. A portion of the product was recrystallized twice-flrst from 50% aqueous dimethyl formamide and then from 50% aqueous dimethyl formamide and then from butyl alcohol-giving the ester in the form of small colorless prisms which melted in the range of 128.6 to 129.9 C.
The crude ester was then slurried for 12 hours at room temperature with 8.9 parts or 50% aqueous alcohol and 1.73 parts of 30% aqueous sodium hydroxide. The resulting solution or the sodium salt of [6-nitro-2-(T-thenoy1) -benzoic} 3'-nitro- 2-(2'-thenowl) -ben'zoic acid was filtered to remove a small amount of alkali msolu-bie material and made strongly acid by the slow addition of excess concentrated hydrochloric acid. The precipitated crystalline [6 nitro 2 (2' thenoyl) benzoic] 3-nitro-2-(2'-theno2/l)-beneoie acid as the free acid was filtered, washed with cold water and dried. The yield was 1.02 parts. equal to 83% of the theoretical.
Example 2 To 1.00 part of 2-carbomethoxy-3-nitrobenzoic acid suspended and agitated- 1112.45 or monochlorobenzene there was. added, carefully canoe and in small portions, 1.02 parts oi phosphorus pentachloride. The reaction was vigorous. Much hydrogen chloride was evolved and the temperature rose slowly to 35 C. at which point all of the starting material had gone into solution. The reaction was completed by heating the charge to 65 C. for several minutes.
The resulting solution or 2-carbomethoxy-3- nitrobenzoyl chloride, containing a molar equivalent of phosphorus oxychloride, was cooled to 8 C. and 1.32 parts of anhydrous stannic chloride were dropped in during about 15 minutes.
The temperature of the charge was adjusted to 10-15 C., and, during 45 minutes, a solution of 0.385 part of thiophene in 2.45 parts of monochlorobenzene was added. After holding the reaction mass at 10-15 C. for a further 45 minutes, it was poured into 9 parts of ice and water. The organic layer was separated and washed with 3% aqueous hydrochloric acid. The resulting [6 nitro 2 (2' thenoyl) benzoic] 3-nitro- 2-(2-thenoyl) -benzoic acid methyl ester crystallized from the organic phase. The yield was 1.03 parts (80% of the theoretical), as measured by the quantity of [6 nitro 2 (2' thenoyl) benzoic] 3-nitro-2-(2-thenOyl)-benzoic acid obtained by hydrolysis of the ester with alkali as described in Example 1.
In the procedure of Example 1, an equivalent quantity of 2-chlorothiophene was substituted for the thiophene. The product, [6-nitro-2-(5'- chloro-2 -thenoyl) -benzoic] 3-nitro-2- (5'-ehloro- 2'-thenoyl) -benzoic acid methyl ester, separated from the steam-distilled mass as a granular solid, which, after two recrystallizations, first from aqueous dimethyl formamide and then from ethyl alcohol, melted in the range of 139.6-140.6 C. As measured by the quantity oi [6-nitro-2-(5'- chloro-2'-thenoyl) -benzoic] 3-nitro-2-(5'-chloro- 2'-thenoyl)-benzo ic acid obtained by hydrolysis of the crude ester, the yield was 0.84 part (58% of the theoretical).
Example 4 In the procedure of Example 1, an equivalent quantity of 2-bromothiophene was substituted for the thiophene. The product, [6-nitro-2-(5'- bromo-2 -thenoyl) -benzoic] 3-mtro-2- (5 -bromo- 2'-thenoyl) -benzoic acid methyl ester, separated from the steam-distilled mass as an oil which solidified on standing. After two recrystallizations from aqueous ethanol, the ester was obtained as a highly crystalline solid which melted at about 135 C. As measured by the quantity of [6-nitro-2-(5'-bromo-2-thenoyl) -benzoic] 3-mtr-2-(5-bromo-2'-thenoyl)-benzoic acid obtained by hydrolysis of the crude ester, the yield was 0.44 part (28% of the theoretical).
Example To 1.00 part of 2-carbomethoxy-5-nitrobenzoic acid suspended and agitated in 2.94 parts of ortho-dichlorobenzene there was added, under 25 C., 1.02 parts of phosphorus pentachloride. After the vigorous reaction had subsided, the charge was allowed to stand at room temperature for about 12 hours. The resulting solution of 2- carbomethoxy-5-nitrobenzyl chloride, containing a molar equivalent of phosphorus oxychloride. was cooled to about 0 C. and 0.68 part of phosphorus oxychloride and 1.32 parts of stannic chloride were added.
The temperature of the charge was readjusted to 0 C. and, during 2 hours and minutes, a solution of 0.385 part thiophene in 2.94 parts of 6 ortho-dichlorobenzene was introduced. After holding the reaction mass at 0 C. for another hour it was poured into 9 parts of ice and water. The organic layer was separated, washed 5 times with dilute aqueous hydrochloric acid, and, finally, steam-distilled free of ortho-dichlorobenzene. The yield of crude product, [4-nitro-2-(2'- thenoyl) -benzoic] S-nitro-Z-(W-thenoyl) -beneoic acid methyl ester, was 1.15 parts. After two crystallizations, first from ortho-dichlorobenzene and then from butanol, the product melted at about C.
Hydrolysis of the crude ester, as described in Example 1, gave 0.86 part (70% of the theoretical) of [=l-nitro-2- (2-thenoyl) -benzoic] 5-nitro-2- (2'-thenoyl)-benzoic acid.
As illustrated by Examples 1 to 5, it is convenient to prepare the acid chloride in situ" by reacting the free acid-either 2-carbomethoxy- (3 or 5) -nitrobenzoic acidwith phosphorus pentaohloride in the desired inert solvent. Thus, a molar equivalent of phosphorus oxychloride is introduced automatically into the reaction system as a consequence of acid chloride formation. This procedure has the important technological advantage of avoiding the otherwise necessary separate step of preparing and isolating the relatively unstable acid chloride. In some cases, particularly when chlorinated inert solvents (such as ortho-dichlorobenzene), are used, it is desirable to add another molar equivalent, or more, of phosphorus oxychloride to the reaction mass to insure homogeneity during condensation,
The process as described in Examples 1 to 5 operates satisfactorily when between 1.0 and 1.5 mole of thiophene per mol of acid chloride are employed. However, with the smaller quantity gf thiophene cleaner products result and. for this reason, 1.0 mol of thiophene per mol of acid chloride represents the preferred usage. Quantities of thiophene in excess of 1.5 mols/mol may be used if desired, but the nitrothenoylbenzoic acid alkyl esters so produced will be contaminated to a greater extent with polymeric impurities.
The length of time during which the thiophene solution is added to the reaction mass is not critical. Entirely satisfactory results are obtained with times of addition varying from 45 minutes to 2 /2 hours. As the condensation reaction is exothermic, such practical considerations as the cooling capacity of the reaction system will determine the optimum addition time- It is preferred to operate the process in such manner that the completed condensation mass contains about 1 part of product (based on the theoretical yield) per 3 to 5 parts of inert solvent, because, under these circumstances, temperature control is obtailned readily and the mass remains fluid so that it may be transferred readily from one piece of equipment to another. Satisfactory operation, however, can he obtained with larger or smaller quantities of solvent.
As inert solvents, aromatic or aliphatic hydrocarbons, aromatic or aliphatic chlorinated hydrocarbons, or aromatic nitrated hydrocarbons may be employed. For example, satisfactory results have been obtained with benzene, monochlorobenzene. orthodichlorobenzene, nitrobenzene, tetrachlorethane and carbon tetrachloride. Preferred solvents are monochlorobenzene and orthodichlorobenzene because they are readily removed and recovered from the reaction mass by steam-distillation and because they present no great fire hazard when employed on a technical scale.
The anhydrous stsnnl'e chloride used may be varied from about (1.155 to 1.1 molsper moi of acid chloride Or more without aitectim greatly either the yield or quality oi the product. The use of amounts of anhydrous stannic chloride larger than 1.1 mols per mol has no advantage. The use of amounts smaller than about .5- mol per mol results in decreased yields.
Preferred condensation temperatures are those between 0 C. and 20 C. Higher temperatures may be used, but a slight decrease in yield is noted when the, temperature is increased too much above 20 C.
The intermediates, 2-carboalkoxy-(3 or 5)-nitrobenzoic acids, are easilyprepared by known methods by reacting the readily available 3- or 4- nitrophthalic anhydrldes with an aliphatic alcohol. Thus, by refluxing 3-nitrophthaiic anhydride with methyl alcohol there is produced 2'- carbomethoxy-3-nitrobenzoic acid which is isolated easily by evaporating excess methyl alcohol from the reaction mass. Similarly, with ethyl alcohol, propyl alcohol and butyl alcohol there is obtained the corresponding 2-carboalkoxy-3-nitrobenzoic acid. The various camboalkoxy nitrobenzoic acids may be converted to the corresponding acid chlorides and reacted with thiophene compounds to produce nitrothenoylbenzoic acid alkyl esters by the methods. given in Examples 1 to 5.
The 2-oarboalkoxy-(3 or 5) -nitrobenzoyi chlorides are synthesized readily by treating the free acids with chlorinating agents such as thionyl chloride or phosphorus pentachioride.
Iclaim:
1. A process for preparing nitro-2-(2'-thenoyl)-benzoic acid alkyl esters which comprises reacting a 2-carboalkoxy-nitrobenzoyl chloride, which carries the nitro group in one oi. the positions 3- and 5- and in which the alkoxy group contains from 1 to 4 carbon atoms, with from 1.0 to 1.5 mols of a thiophene, compound of the class consisting of thiophene, 2-chlorothiophehe and 2-bromothiophene, in an inert organic solvent in the presence of 0.55 to 1.1 mol of anhydrous stannic chloride and at least 1 mol of phosphorus oxychloride, per mol of carboalkoxy-nitrobenzoyl chloride employed, the reaction being carried out at temperatures of from 0 to 20 C.
2. The process of claim 1 in which the thiophene compound is slowly added. to the inert organic solvent solution of the. carboalkoxwbenzoyl chloride, anhydrous stannic chloride and phosphorus oxychloride.
3. A process for preparing [6-nitro-2-(2'- thenoyil manhole} 3- nitro-- 2-(2'-the'*noyl)benzoic acid methyl ester which comprises reacting the 2-earbomethoxy-ii-nitrobenzoyl chloride with from 1.0 to 1.5 mols of thiophene in an inert organic solvent and in the presence of 0.55 to 0.1 mol of anhydrous stannic chloride and at least 1 mol of phosphorus oxychloride, per mol of the carbomethoxy-nitrobenzoyl chloride employed. the reaction being carried out at temperatures of from 0 to 20 C.
4. The process of claim 3 in which the thiophone is slowly added to the inert organic solvent solution of the carbomethoxy-nitrobenz'oyl chloride, anhydrous stannic chloride and phosphorus oxychlcrlde.
5'. The nitro-2-(2'-thenoyl) -benzolc acid alEyl esters of the formula:
in which one of the [substitutents] substituents Y and Z' is a N0: group and the other is'hydrogen'.
and wherein X is a [substitutent] substitucnt o! oyl) -ben2oic acid methyl ester.
8. [4-nitro-2-(2'-thenoyl) -benzoic acid methyl esterJ'b' m'tm 2-(2' thenoyU-beneoic acid methyl ester.
EDWARD K. GLADDlNGr REFERENCES CITED The following references are of record in the file of this patent or the original patent:
Smorganskii and Goldfarb, Chem. Abst. 35 :4011 (1941) Certificate of Correction Reissue No. 23,405 September 4, 1951 EDVARD K. GLADDING It is hcrehy certified that orror appears in the printed specification of the above numbcl'ml patcnt requiring corrm-tion as follows:
Column 3, line 43, 3-nitro-2-(2-thcno vl) should he italics 3-11112042- (E'Jhenoyl) column 5. between lines 28 and 29, insert the heading Example 3 .7 line 68, for nitrobenzyl" read nitrobcnzoyl column 6, llne 59, for obtailncd read obtained and that the said Letters Patent should be read as corrected above, so that the same may conform to the record of the case in the Patent Office.
Signed and sealed this 13th day of November A. D. 1951.
[SEAL] THOMAS F. MURPHY,
Assistant Commissioner of Patents.
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