Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 2022; 33(16): 1670-1674
DOI: 10.1055/a-1887-7885
DOI: 10.1055/a-1887-7885
letter
Aerobic Photooxidation of Toluene Derivatives into Carboxylic Acids with Bromine–Water under Catalyst-Free Conditions
Abstract
The photoirradiation of toluene derivatives with two equivalents of bromine in benzotrifluoride–water provided a satisfactory yield of the corresponding benzoic acid derivatives. Either a fluorescent lamp, blue LED (454 nm), or UV LED (385 nm) was used for the photoreaction. The reaction pathway might proceed through the dibromination of benzylic carbon, generation of the benzylic radical via oxidative C–H abstraction, formation of benzoyl bromide, and hydrolysis of carboxylic acid.
Key words
oxidation - toluene - benzoic acid - carboxylic acid - bromine - aerobic oxidation - photoreactionSupporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/a-1887-7885.
- Supporting Information
Publication History
Received: 27 May 2022
Accepted after revision: 29 June 2022
Accepted Manuscript online:
29 June 2022
Article published online:
26 July 2022
© 2022. Thieme. All rights reserved
Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany
-
References and Notes
- 1a Ullmann HM. Am. Chem. J. 1894; 16: 530
- 1b Bigelow LA. J. Am. Chem. Soc. 1922; 44: 2010
- 1c Gannon SM, Krause JG. Synthesis 1987; 915
- 1d Li W.-S, Liu LK. Synthesis 1989; 293
- 1e Zhao D, Lee DG. Synthesis 1994; 915
- 1f Shaabani A, Lee DG. Tetrahedron Lett. 2001; 42: 5833
- 1g Pan J.-F, Chen K. J. Mol. Catal. A: Chem. 2001; 176: 19
- 1h Semenok D, Medvedev J, Giassafaki L.-P, Lavdas I, Vizirianakis IS, Eleftheriou P, Gavalas A, Petrou A, Geronikaki A. Molecules 2019; 24: 1751
- 2a Rangarajan R, Eisenbraum EJ. J. Org. Chem. 1985; 50: 2435
- 2b Pearson AJ, Han GR. J. Org. Chem. 1985; 50: 2791
- 2c Rathore R, Saxena N, Chandrasekaran S. Synth. Commun. 1986; 16: 1493
- 2d Muzart J. Tetrahedron Lett. 1986; 27: 3139
- 2e Muzart J. Tetrahedron Lett. 1987; 28: 2131
- 2f Choudary BM, Prasad AD, Bhuma V, Swapna V. J. Org. Chem. 1992; 57: 5841
- 2g Das TK, Chaudhari K, Nandanan E, Chandwadkar AJ, Sudalai A, Ravindranathan T, Sivasanker S. Tetrahedron Lett. 1997; 38: 3631
- 2h Rothenberg G, Wiener H, Sasson Y. J. Mol. Catal. A: Chem. 1998; 136: 253
- 3a Kitajima N, Sunaga S, Moro-oka Y, Yoshikuni T, Akada M, Tomotaki Y, Taniguchi M. Bull. Chem. Soc. Jpn. 1988; 61: 967
- 3b Kitajima N, Takemura K, Moro-oka Y, Yoshikuni T, Akada M, Tomotaki Y, Taniguchi M. Bull. Chem. Soc. Jpn. 1988; 61: 1035
- 3c Hirai N, Sawatani N, Nakamura N, Sakaguchi S, Ishii Y. J. Org. Chem. 2003; 68: 6587
- 3d Lee JS, Hronec M, Lee KH, Kwak JW, Chu YH. WO2008111764, 2008 ; Chem. Abstr. 2008, 149, 379148
- 3e Bhattacharyya A US20140100386, 2014 Chem. Abstr. 2014, 160, 544899
- 3f Fukuhara H. EP818433, 1998 ; Chem. Abstr.1998, 128, 140522
- 3g Nakai T, Iwai T, Mihara M, Ito T, Mizuno T. Tetrahedron Lett. 2010; 51: 2225
- 3h Yang F, Sun J, Zheng R, Qiu W, Tang J, He M. Tetrahedron 2004; 60: 1225
- 4a Sugai T, Itoh A. Tetrahedron Lett. 2007; 48: 9096
- 4b Itoh A, Hashimoto S, Kodama T, Masaki Y. Synlett 2005; 2107
- 4c Zheng K, Yan X, Zhang G, Yan X, Li X, Xu X. Synlett 2020; 31: 272
- 4d Hirashima S, Itoh A. Synthesis 2006; 1757
- 4e Moriyama K, Takemura M, Togo H. Org. Lett. 2012; 14: 2414
- 4f Hirashima S, Itoh A. Photochem. Photobiol. Sci. 2007; 6: 521
- 4g Sugai T, Itoh A. Tetrahedron Lett. 2007; 48: 2931
- 5a Rabjohn N. J. Am. Chem. Soc. 1954; 76: 5479
- 5b Onogawa Y, Takao Y, Kusagaya K, Furusawa O. JP2001114741, 2001 ; Chem. Abstr. 2001, 134, 295621
- 5c Warashina T, Matsuura D. JP2019156766, 2019 ; Chem. Abstr. 2019, 171, 385169.
- 6 Coleman GH, Honeywell GE. Org. Synth. 1937; 17: 20
- 7 Bromination of toluene under a 60 W fluorescent lamp: Itoh A, Masaki Y. Synlett 1997; 1450
- 8 Bromination of 4-fluorotolune with BPO: Men, X. CN110655457, 2020; Chem. Abstr. 2021, 173, 473693.
- 9 Bromination of toluene with KBr–Oxone: Zhao M, Li M, Lu W. Synthesis 2018; 50: 4933
- 10 Typical Experimental Procedure A 100 mL Pyrex flask was charged with 1-cyano-4-methylbenzene ( p-1a, 586 mg, 5.0 mmol) and Br2 (840 mg, 10.5 mmol) in BTF (30 mL) and water (6 mL). The attached reflux condenser was open air, and the flask was irradiated with a 13 W white fluorescent lamp at intervals of 5 cm with vigorous stirring for 24 h. The reaction mixture was combined with saturated aqueous NaHCO3 and EtOAc. The alkaline aqueous layer was then separated and acidified with diluted HCl. The solution was successively extracted using EtOAc and washed with H2O and brine. After drying over anhydrous Na2SO4, it was concentrated to produce 4-cyanobenzoic acid ( p-2a, 684 mg, 93%) colorless crystals. The sample was sufficiently pure, and further purification was not performed. 4-Cyanobenzoic Acid (p-2a) Mp 222 °C (lit.11 mp 221 ℃). 1H NMR (400 MHz, CD3OD): δ = 8.11 (d, J= 8.4 Hz, 2 H), 7.79 (d, J = 8.4 Hz, 2 H). 13C NMR (101 MHz, CD3OD): δ = 167.9, 135.9, 133.3, 131.2, 118.9, 117.1.
- 11 Rhee H, An G, Ahn H, De Castro K. Synthesis 2010; 477
Oxygen oxidation of toluene derivatives to the aldehydes:
Oxygen oxidation of p-1a to p -2a:
Oxygen oxidation of p-1i to p-2i: