HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238695Generated: October 26, 2026
3-Carboxyphenylboronic acid → 2'-Methoxy-3'-nitrobiphenyl-3-carboxylic acid
https://huagongshe.com/reaction/238695
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Carboxyphenylboronic acid | HCID 2733957 | — |
| Reactant | 1-Bromo-2-methoxy-3-nitrobenzene | HCID 22505713 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2'-Methoxy-3'-nitrobiphenyl-3-carboxylic acid | HCID 9856767 | 197.4% |
Reaction Steps
1-Bromo-2-methoxy-3-nitro-benzene 1c (23.25 g, 0.10 mol), 3-carboxyphenylboronic acid (19.5 g, 117 mmol) and tetrakis(triphenylphosphine)palladium (8.86 g, 7.7 mol) were dissolved in a solvent mixture of 100 mL of 2 M sodium carbonate solution and 500 mL of 1,4-dioxane. The reaction mixture was heated to reflux at 105° C. for 43 hours. The mixture was concentrated under reduced pressure and then 300 mL of 6 N hydrochloric acid and 400 mL of ethyl acetate were added. The aqueous layer was extracted with ethyl acetate (200 mL×2). The combined organic extracts were dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated under reduced pressure to obtain the title compound 2′-methoxy-3′-nitro-biphenyl-3-carboxylic acid 1d (53.93 g) as a light yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642637B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-19e50ae11ac44868a31d61a5fc13bd02 |
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| Source note | uspto-grants-2014_02 |
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