RU2800099C1 - Method of obtaining aminophenols - Google Patents

Abstract

FIELD: organic chemistry.

SUBSTANCE: invention relates to the synthesis of ortho- and para-aminophenols, which are important raw materials for the chemical and pharmaceutical industries. The invention relates to organic chemistry, specifically to a method of producing ortho- and para-aminophenols by aniline oxidation in an alkaline medium and subsequent hydrolysis of intermediate 4(2)-aminophenyl sulfates with hydrochloric acid at 85–95°C, characterized by the following: the synthesis is carried out without isolation of intermediate 4(2)-aminophenyl sulfates, and aniline is oxidized with ammonium persulfate (PSA), or sodium (PSN), or potassium (PSK) and hydrogen peroxide as the second oxidizing agent at the molar ratio of Aniline:NaOH:PSA(PSN, PSK):H₂O₂, equal to 1:5: 1.5:2, temperature 40–50°C for 2–15 hours.

EFFECT: increasing the yield of target products.

1 cl, 5 tbl, 1 ex

Description

The invention relates to organic chemistry, specifically to the synthesis of ortho- and para-aminophenols, which are important raw materials for the chemical and pharmaceutical industries. Thus, ortho-aminophenol is used as a dye for fur, in photography as a developer, and in the synthesis of certain drugs. Para-aminophenol is used as a component of dyes for fur, a black-and-white developer in photography, and in the synthesis of drugs, in particular paracetamol.

A two-stage method for producing ortho- and para-aminophenols is known. At the first stage, the nitration of phenol is carried out, at the second stage, the corresponding nitrophenol is reduced in the presence of iron filings in an acidic environment (A.E. Chichibabin “Basic Principles of Organic Chemistry”, vol. II).

Nitrophenols, in turn, can be obtained by nitration of phenol [US 3663261 (1973), US 3517075 (1971), US 3510527 (1971)], cumene hydroperoxide [US 3388173 (1968)], from nitrochlorobenzene [US 3263011 (1966)], oxidation of nitrosophenol [pat . CPP 53445 (1971), RU 2076095 (1997)].

So, when phenol is nitrated with a nitrating mixture consisting of nitric, sulfuric acids and nitrogen oxides [US 3663261 (1973), US 3517075 (1971)] or liquid nitrogen oxides in nitric acid [US 3510527 (1971)], a mixture of ortho- and para-nitrophenols is obtained with a yield of 17 and 73%, respectively. The disadvantage of this method is the use of toxic nitrogen oxides.

When cumene hydroperoxide is nitrated with a mixture of nitric acid and nitrogen oxides in chloroform, a mixture of ortho- and para-nitrophenols is also obtained with yields of 30 and 7%, respectively [US 3388173 (1968)]. The disadvantages of this method, along with the use of toxic nitrogen oxides, is the use of unstable cumene hydroperoxide, as well as the need to separate ortho- and para-nitrophenols by steam distillation.

According to [US 3263011 (1966)], when 4- or 2-nitrochlorobenzenes are heated in an autoclave in a 2-4% aqueous solution of alkali at 160°C with continuous air blowing, the corresponding nitrophenol is obtained. The disadvantage of this method for obtaining nitrophenols is the process under pressure, as well as the non-selectivity of nitration of chlorobenzene, which requires the separation of ortho- and para-isomers by steam distillation.

Para-nitrophenols can also be obtained by oxidation of para-nitrosophenol. So, according to [US Pat. CPP 53445 (1971)] para-nitrosophenol is oxidized with nitric acid, and according to [RU 2076095 (1997)] - with 33% hydrogen peroxide in the presence of Na ₂ WO ₄ ⋅2H ₂ O catalyst. in the second, an expensive and toxic catalyst is used.

Para-nitrosophenol can be reduced to para-aminophenol in ethyl acetate in the presence of a Pd/C catalyst at a hydrogen pressure of 2.0–4 atm and a temperature of 20–50°C [RU 2461543 (2012)]. The disadvantage of the method is the process under pressure, the use of an expensive catalyst (Pd), as well as environmentally unsafe solutions of concentrated acids (HCl, HNO ₃ ) and alkalis.

A known method for producing aminophenols by photooxidation of aromatic amines with oxygen by irradiation with visible light in an aqueous organic solvent in the presence of active and stable photosensitizers, which are substituted phthalocyanines [RU 2567552 (2015)]. The yield of p-aminophenol is 70%. However, this method involves the use of complex special equipment - a laser or LEDs.

The closest to the claimed method for obtaining ortho- and para-aminophenols is a two-stage process, in the first stage of which aniline is oxidized with ammonium persulfate in an alkaline medium at 40-60 ° C, in the presence of 0.01-0.03 wt% phthalocyanine oxidation catalyst (phthalocyanine cobalt, iron (II), iron (III), manganese, nickel or zinc), followed by cooling the reaction mixture, isolation of intermediate 4(2)-aminophenyl sulfates. By hydrolysis of the latter in an acidic medium at 85-95°C, a mixture of ortho- and para-aminophenols is obtained, from which ortho-aminophenol is isolated by extraction with chloroform. Para-aminophenol remains in the aqueous phase. Depending on the duration of aniline oxidation, the yield and ratio of the formed ortho- and para-isomers varies. The maximum yield of para-aminophenol (72%) is achieved when the duration of aniline oxidation is 15 h, while ortho-aminophenol (13%) is also isolated from the reaction mixture (RF Patent Application No. 2021130569).

The problem to be solved by the present invention is to increase the yield of target compounds.

The problem is solved by the proposed one-pot method for obtaining ortho- and para-aminophenols. Aniline is oxidized with ammonium persulfate (PSA) or potassium (PSK) or sodium (PSN) and hydrogen peroxide as the second oxidizing agent, in an alkaline medium at a molar ratio of Aniline:NaOH:PSA (PSK, PSN):H ₂ O ₂ equal to 1:5:1.5:2.0 at 40-50 ° C for 2-18 hours. Then the reaction mixture is cooled to room temperature, hydrochloric acid is hydrolyzed oh at 85-95 ° C and a mixture of o- and p-aminophenols is obtained, from which o-aminophenol (o-AF) is isolated by extraction with chloroform (yield up to 30%), p-aminophenol (p-AF) remains in the aqueous phase (yield up to 75%). It should be noted that the duration of aniline oxidation (2–15 h) affects the ratio of ortho- and para-aminophenols isolated after hydrolysis of intermediate 4(2)-aminophenyl sulfates (table). Thus, during the oxidation of aniline for 15 h, only one isomer, para-aminophenol, was isolated from the reaction mixture in a 75% yield (Table 1, p. 6).

The essence of the claimed technical solution is confirmed by examples of a specific implementation.

Example 1. Obtaining ortho- and para-aminophenols (Table 1, p. 3)

In a three-necked flask equipped with a dropping funnel, a reflux condenser and a mechanical stirrer, 5 ml (0.055 mol) of aniline is stirred in 30 ml of distilled water at 40 ° C until the aniline is completely dissolved, then a solution of 11 g of NaOH (0.275 mol) in 70 ml of water is added dropwise to the reaction mixture and a solution of 18.7 g (0.082 mol) of persulfate is added dropwise ammonium in 40 ml of water. After complete addition of ammonium persulfate, 10 ml of 30% hydrogen peroxide (0.11 mol) are added dropwise. The reaction mixture was stirred at 40°C for 6 h, cooled to room temperature, extracted with ethyl acetate (2×30 ml) to remove unreacted aniline. 3.34 ml (0.11 mol) of hydrochloric acid are added dropwise to the aqueous fraction, heated to 90°C and kept at this temperature with constant stirring for 3 h, controlled by TLC (eluent ethanol:ammonia 4:1), cooled to room temperature, alkalized with NaHCO ₃ solution to pH 7-8, extracted with chloroform (3×20 ml), the organic layer is dried MgSO ₄ , after removing the solvent, 1.8 g (30%) of ortho-aminophenol are obtained in the form of dark brown crystals. In terms of the original aniline, the yield of ortho-aminophenol is 30%.

Ortho-aminophenol (3). Crystals of dark brown flowers. T _pl =172-175°C. ^1Н NMR spectrum (CDCl ₃ , δ, ppm): 4.4 (2Н, br. s, NH ₂ ), 6.42 (1Н, m, H-5), 6.54-6.58 (2Н, m, ArH), 6.64 (1Н, m, H-6). ^13С NMR spectrum (CDCl ₃ , δ, ppm): 115.21 (C-6), 116.17 (C-3), 118.98 (C-4), 120.47 (C-5), 134.02 (C-NH ₂ ), 144.62 (C-OH).

The aqueous phase is evaporated to dryness, the residue is dissolved in ethyl alcohol, the ethanol extract is evaporated under reduced pressure and 1.2 g (20%) of para-aminophenol are obtained in the form of light brown crystals. In terms of the original aniline, the yield of para-aminophenol is 20%.

Para-aminophenol (4). Light brown crystals. T _pl =185-188°C. ^1Н NMR spectrum (DMSO-d ₆ , δ, ppm): 4.37 (2Н, br. s, NH ₂ ), 6.37-6.44 (2Н, m, ArH), 6.44-6.50 (2Н, m, ArH), 8.33 (1Н, br. s, OH). ^13С NMR spectrum (DMSO-d ₆ , δ, ppm): 115.90, 116.08 (4 CH, ArH), 140.97 (C-NH ₂ ), 148.80 (C-OH).

Table 1. Dependence of the yield of ortho- and para-aminophenols on the duration of oxidation, the oxidizing agent is ammonium persulfate (molar ratio of aniline:NaOH:PSA:H ₂ O ₂ 1:5:1.5:2; temperature 40°C) No. p / p Reaction time, h AF output, % general o-AF p-AF 1 2 28 20 8 2 4 43 thirty 13 3 6 50 thirty 20 4 8 56 13 41 5 10 60 10 50 6 15 75 - 75 7 18 72 - 72

Table 2. Dependence of the yield of ortho- and para-aminophenols on the duration of oxidation, the oxidizing agent is potassium persulfate (molar ratio of aniline:NaOH:PSA:H ₂ O ₂ 1:5:1.5:2; temperature 40°C) No. p / p Reaction time, h AF output, % general o-AF p-AF 1 2 23 18 5 2 4 35 25 10 3 6 40 25 15 4 8 42 17 thirty 5 10 52 8 44 6 15 68 - 68 7 18 65 - 65

Table 3. Dependence of the yield of ortho- and para-aminophenols on the duration of oxidation, oxidizing agent - sodium persulfate (molar ratio of aniline:NaOH:PSN:H ₂ O ₂ 1:5:1.5:2; temperature 40°C) No. p / p Reaction time, h AF output, % general o-AF p-AF 1 2 20 15 5 2 4 29 22 7 3 6 35 23 12 4 8 37 eleven 26 5 10 46 6 40 6 15 60 - 60 7 18 58 - 58

Table 4. Dependence of the yield of ortho- and para-aminophenols on the temperature and duration of oxidation, the oxidizing agent is ammonium persulfate (molar ratio of aniline:NaOH:PSA 1:5:1.5) * No. p / p Reaction time, h Temperature, °С AF output, % general o-AF p-AF 1 15 20 12 6.5 5.5 2 5 40 18 eleven 7 3 15 40 35 18 17 4 5 50 18 10 8 5 15 50 33 16 17 6 5 60 15 9 6 7 15 60 25 12 13 * - the reaction was carried out without adding H ₂ O ₂

Table 5. Dependence of the yield of ortho- and para-aminophenols on the amount of hydrogen peroxide, oxidant - ammonium persulfate (molar ratio of aniline:NaOH:PSA 1:5:1.5; temperature 40°C; time - 15 h) No. p / p Aniline:H ₂ O ₂ ratio, mol AF output, % general o-AF p-AF 1 1:0 18 12 6 2 1:0.5 50 15 35 3 1:1 60 7 53 4 1:1.5 72 - 72 5 1:2 75 - 75 6 1:2.5 73 - 73

Thus, a method has been proposed for the production of ortho- and para-aminophenols, which makes it possible to increase the yield of easily separable target ortho- and para-aminophenols, the ratio of which can be varied depending on the duration of aniline oxidation.

Claims (1)

A method for obtaining ortho- and para-aminophenols by oxidizing aniline in an alkaline medium and subsequent hydrolysis of intermediate 4(2)-aminophenyl sulfates with hydrochloric acid at 85-95°C, characterized in that the synthesis of target ortho- and para-aminophenols is carried out without isolation of intermediate 4(2)-aminophenyl sulfates, and aniline is oxidized with ammonium persulfate (PSA), or sodium (PSN), or potassium (P SK) and hydrogen peroxide as the second oxidizing agent at a molar ratio of Aniline:NaOH:PSA(PSN, PSK):H ₂ O ₂ equal to 1:5:1.5:2, at a temperature of 40-50°C for 2-15 hours.