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Coupling of 2-bromobenzoic acid with 4-methoxythiophenol under Ullmann conditions; 2-((4-Methoxyphenyl)thio)benzoic acid

SyntheticPage 846
DOI: 10.1039/SP846
Submitted Aug 23, 2018, published Oct 15, 2018
Robert Smith (, Mariyah Sajjad (), Mark Wainwright (, Joshua Gettins ()
A contribution from Smith Group

			Reaction Scheme: <IMG src="/images/empty.gif"><IMG alt="" src="/images/empty.gif">Coupling of <SPAN id=csm1547225500421 title="2-bromobenzoic acid" class=csm-chemical-name grpid="1">2-bromobenzoic acid</SPAN> with <SPAN id=csm1547225506699 title=4-methoxythiophenol class=csm-chemical-name grpid="2">4-methoxythiophenol</SPAN> under Ullmann conditions<IMG alt="" src="/images/empty.gif"><IMG src="/images/empty.gif">

Chemicals Used

2-Bromobenzoic Acid (Sigma Aldrich)

4-Methoxythiophenol (Sigma Aldrich)

Anhydrous potassium carbonate (Sigma Aldrich)

100 mesh copper bronze (Alfa Aesar)


A mixture of 2-bromobenzoic acid (10.63 g, 52.9 mmol), 4-methoxythiophenol (6.57 g, 52.9 mmol), K2CO3 (14.60 g, 105.8 mmol) and powdered Cu bronze (1.71 g, 26.44 mmol) in DMF (100 mL) was stirred at reflux for 6 hours. Upon cooling, the reaction mixture was poured into ice (500 g) and acidified with concentrated HCl to pH=4 giving a white solid.  The solid was isolated and dried at the vacuum pump** to yield 2-((4-methoxyphenyl)thio)benzoic acid (6.10 g, 44%) as a white solid.

Author's Comments

*** Round bottom flask fitted with a reflux condenser was used which fitted snuggly into a metal heating block.  A thermocouple was used to control the temperature and reaction was open to the air (no inert gasses were required).  Stirring was accomplished using a stirring bar which was controlled from the hot plate.  The whole reaction was accomplished in the open air without the need of dry/inert conditions.
** pH determined using universal indicator paper.
***No purification required, but the authors suggest holding the compound at the vacuum pump for at least an hour until dry.


1H NMR (400 MHz, DMSO-d6) δ 13.27 (s, 1H), 7.93 (dd, J = 7.7, 1.5 Hz, 1H), 7.47 (d, J = 8.5 Hz, 2H), 7.36 – 7.29 (m, 1H), 7.15 (td, J = 7.5, 1.2 Hz, 1H), 7.06 (d, J = 8.6 Hz, 2H), 6.65 (dd, J = 8.3, 1.2 Hz, 1H), 3.81 (s, 3H). 13C NMR (101 MHz, DMSO) δ 167.80, 160.80, 143.95, 137.89, 132.81, 131.42, 127.13, 126.37, 124.57, 122.41, 116.15, 55.77. MS m/z: 261.02 [M+].

Lead Reference

Wang, C., Jiang, H., Jin, J., Xie, Y., Chen, Z., Zhang, H., Lian, F., Liu, Y.-C., Zhang, C., Ding, H., Chen, S., Zhang, N., Zhang, Y., Jiang, H., Chen, K., Ye, F., Yao, Z., Luo, C. 
Development of Potent Type i Protein Arginine Methyltransferase (PRMT) Inhibitors of Leukemia Cell Proliferation 
Journal of Medicinal Chemistry, (2017): 60 (21), pp. 8888-8905.

Supplementary Information

1H - 19862-91-0.pdf
13C - 19862-91-0.pdf
135DEPT - 19862-91-0.pdf
135DEPT vs 13C - 19862-91-0.pdf
1H1H COSY- 19862-91-0.pdf
MS - 19862-91-0.pdf

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Get structure file (.cdx, .sk2, .mol)

Keywords: aromatics/arenes, carboxylic acids, nucleophilic, thiol, Ullmann

Post new comment
  • Registered user Susan Elizabeth RichardsonJan 11 2019 2:43PM

    Just marking up the compounds here, and I've noticed that the reaction scheme depicts 4-methoxythiophenol, the product is a thioether, but the text repeatedly mentions 4-methoxyphenol. Should the text be amended to 4-methoxythiophenol?

    • Guest Robert B SmithJan 11 2019 3:11PMCorrection

      Please if this could be changed. Thanks for sorry for the typo. Rob

      • Registered user Susan Elizabeth RichardsonJan 11 2019 4:47PM

        Now changed!

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