The effect of microwave irradiation on the intermolecular and intramolecular Friedel - Crafts acylation of aromatic compounds was investigated. Microwave irradiation had no effect on the intermolecular reaction but had an accelerating effect on the intramolecular reaction. This enhanced intramolecular reactivity that was attributed to the high probability of close proximity between the reaction sites.
The Friedel-Crafts acylation of an aromatic compound introduces an acyl group into the aromatic ring to form a new carbon-carbon bond [
In recent years, many studies have examined the reaction accelerating effect of microwave irradiation [
In this study, we investigated the effect of microwave irradiation on the acylation of naphthalenes. The rate constants were compared for reactions performed under microwave irradiation conditions and under conventional heating conditions. Similarly, the effect of microwave irradiation on the intramolecular Friedel-Crafts cyclization of benzene derivatives was examined.
Substituted naphthalenes and 3-phenylpropanoyl chloride were purchased commercially.
Synthesis of 4-Phenylbutyloyl ChlorideTo a round-bottom flask, 4-phenylbutanoic acid (25.0 g, 152 mmol) and thionyl chloride (90.4 g, 760 mmol) were added and then refluxed for 3 h. After completion of the reaction, thionyl chloride was removed by distillation to obtain the desired product. Yield: 26.9 g (96.7%). 1H NMR (400 MHz, CDCl3) δ 7.24 (d, 2H), 7.15 (t, 2H), 7.08 (t, 1H), 2.84 (t, 2H), 2.56 (t, 2H), 1.94 (quin, 2H).
To a 200 mL three-necked flask, 1-methylnaphthalene (3.45 mmol), aluminum chloride (692 mg, 5.18 mmol), acetyl chloride (271 mg, 3.45 mmol) or benzoyl chloride (485 mg, 3.45 mmol) as an acylating reagent, and 5 mL of 1,2-dichloroethane were added. The mixture was refluxed under microwave irradiation and stirred while sampling at regular intervals. Microwave irradiation was performed using a single-mode microwave reactor (μ-reactor: Shikoku Keisoku Ltd.). The power was 500 W operated at 2.45 GHz, and the temperature was measured using an optical fiber thermometer. After washing the sample with sodium bicarbonate, the ratio of substrate to product was measured using HPLC. The experiments using 2-methylnaphthalene, 2-chloronaphthalene, and 1-nitronaphthalene as reaction substrates were performed in the same manner.
Each experiment under conventional heating conditions was conducted using the same reaction mixture in the same flask. The reaction was performed under reflux conditions.
1-Acetyl-4-methylnaphthalene: 1H NMR (400 MHz, CDCl3) δ 8.70 (d, 1H), 7.77 (d, 1H), 7.56 (d, 2H), 7.40 (t, 1H), 7.33 (t, 1H), 7.06 (d, 1H), 2.65 (s, 3H), 2.54 (s, 3H).
1-Benzoyl-4-methylnaphthalene: 1H NMR (400 MHz, CDCl3) δ 9.15 (d, 1H), 7.85 (d, 1H), 7.70 (d, 2H), 7.65 (d, 1H), 7.54 (t, 1H), 7.48 (t, 1H), 7.77 (t, 1H), 7.32 (t, 2H), 7.22 (d, 1H), 2.64 (s, 3H).
2-Acetyl-6-methylnaphthalene: 1H NMR (400 MHz, CDCl3) δ 8.22 (s, 1H), 7.82 (d, 1H), 7.71 (d, 1H), 7.53 (d, 1H), 7.46 (s, 1H), 7.37 (d, 1H), 2.53 (s, 3H), 2.45 (s, 3H).
2-Benzoyl-6-methylnaphthalene: 1H NMR (400 MHz, CDCl3) δ 8.03 (s, 1H), 7.72 (d, 2H), 7.70 (d, 1H), 7.61 (d, 1H), 7.55 (d, 1H), 7.49 (s, 1H), 7.38 (t, 2H), 7.33 (t, 1H), 7.30 (d, 1H), 2.45 (s, 3H).
To a 200 mL three-necked flask, 4-phenylbutanoyl chloride (3.45 mmol), aluminum chloride (692 mg, 5.18 mmol), and 5 mL of 1,2-dichloroethane were added. During reflux by microwave irradiation, sampling was performed at regular intervals. Subsequently, the sample was washed with sodium bicarbonate and analyzed by HPLC. The microwave irradiation and temperature measurements were performed in a manner similar to that described for the intermolecular reactions. The experiment using 3-phenylpropanoyl chloride as the reaction substrate was performed in the same manner.
Under conventional heating conditions, the same reaction mixture and flask were used. The reaction was performed under reflux conditions.
3,4-Dihydro-1(2H)-naphthalenone: 1H NMR (400 MHz, CDCl3) δ 7.86 (d, 1H), 7.40 (t, 1H), 7.21 (d, 1H), 7.15 (t, 1H), 2.56 (t, 2H), 2.55 (t, 2H), 1.84 (m, 2H).
1-Indanone: 1H NMR (400 MHz, CDCl3) δ 7.82 (d, 1H), 7.37 (t, 1H), 7.18 (d, 1H), 7.14 (t, 1H), 2.86 (t, 2H), 2.72 (t, 2H).
The instrumentation and methods used for 1H NMR and HPLC characterization were the same as described in a previous paper [
To compare the results under microwave irradiation conditions and conventional heating conditions, the reactions were performed under the same conditions as much as possible. To achieve the same reaction temperature, all reactions were carried out under reflux conditions.
The Friedel–Crafts acetylation and benzoylation of naphthalenes were investigated. 1-Acyl-4-methylnaphthalene was obtained as the main product from 1-methylnaphthalene, and 2-acetyl-6-methylnaphthalene was obtained from 2-methylnaphthalene [
As shown in
| Substrate | Acylation reagent | K(MW) × 103 (L∙mol−1∙s−1) | K(CH) × 103 (L∙mol−1∙s−1) |
|---|---|---|---|
| 1-methylnaphthalene | acetyl chloride | 42 | 45 |
| 1-methylnaphthalene | benzoyl chloride | 4.4 | 3.9 |
| 2-methylnaphthalene | acetyl chloride | 32 | 29 |
| 2-methylnaphthalene | benzoyl chloride | 0.8 | 0.7 |
| 2-chloronaphthalene | acetyl chloride | 4.3 | 4.3 |
| 1-nitronaphthalene | acetyl chloride | 0 | 0 |
| 1-nitoronaphthalene | benzoyl chloride | 0 | 0 |
acetylation and benzoylation reactions showed that the acetylation reaction proceeded more easily, as is generally known. Similarly, no significant differences were observed between conventional heating and microwave irradiation for the reactions of 2-methylnaphthalene.
Similarly, with 2-chloronaphthalene, which is slightly less reactive, no microwave accelerating effect was observed for the acetylation reaction. With 1-nitronaphthalene, which is known to be less reactive than the other reaction substrates, the reaction did not proceed under either acetylation or benzoylation conditions.
The intramolecular Friedel-Crafts reactions of 4-phenylbutanoyl chloride and 3-phenylpropanoyl chloride gave 3,4-dihydro-1(2H)-naphthalenone and 1-indanone, respectively.
As shown in
In the intermolecular Friedel-Crafts reactions investigated in this study, no reaction accelerating effect was observed. In contrast, a reaction accelerating effect was observed for the intramolecular Friedel-Crafts reactions.
In general, the major difference between an intermolecular reaction and an intramolecular reaction is the magnitude of the entropy change, as an intermolecular reaction in which two molecules react has a more negative activation entropy [
| Substrate | K(MW) × 104 (s−1) | K(CH) × 104 (s−1) |
|---|---|---|
| 3,4-dihydro-1(2H)-naphthalenone | 28 | 21 |
| 1-hydroindone | 7.3 | 4.2 |
intramolecular reaction, there is a high probability that the reaction sites will approach each other. In other words, in an intramolecular reaction, an accelerating effect was observed because the microwave energy could be absorbed by the state in which the reaction sites were close to each other.
The effect of microwave irradiation on intermolecular and intramolecular Friedel-Crafts acylation reactions was examined. The acylation of naphthalenes was used as a model intermolecular reaction, whereas the cyclization on benzene derivatives was used as a model intramolecular reaction. In comparison with conventional heating conditions, microwave irradiation was found to have no accelerating effect on the intermolecular Friedel-Crafts reaction, whereas an accelerating effect was observed for the intramolecular Friedel-Crafts reaction. This effect was attributed to microwave irradiation increasing the probability that the reaction sites were in close proximity to each other in the transition state for the intramolecular reaction.
The authors declare no conflicts of interest regarding the publication of this paper.
Okada, Y. and Fujitsu, A. (2020) Microwave Irradiation Effect on Intermolecular and Intramolecular Friedel-Crafts Acylation Reaction. Green and Sustainable Chemistry, 10, 18-23. https://doi.org/10.4236/gsc.2020.101002