HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820197Generated: October 29, 2026
Toluene → 2'-Ureidobiphenyl-3-carboxylic acid
https://huagongshe.com/reaction/1820197
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (2-Bromophenyl)urea | HCID 139386 | — |
| Reactant | 3-Carboxyphenylboronic acid | HCID 2733957 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2'-Ureidobiphenyl-3-carboxylic acid | HCID 57889050 | 97% |
Reaction Steps
3-Carboxyphenyl boronic acid (100 mg, 0.60 mmol), 2-bromophenyl urea (130 mg, 0.60 mmol), tetrakis(triphenylphosphine)palladium(0) (35 mg, 0.030 mmol), sodium carbonate (192 mg, 1.81 mmol), toluene (5 mL), water (3 mL), and ethanol (3 mL) were mixed at 25° C. under nitrogen then heated in a microwave reactor for 30 minutes at 100° C. Water (5 mL) was added followed by removal of the EtOH in vacuo. The aqueous layer was washed with diethyl ether (2×) and the pH was adjusted to 3 with 1N HCl. The aqueous layer was extracted with ethyl acetate (2×) and the combined were dried over sodium sulfate and then concentrated in vacuo to give 2′-ureidobiphenyl-3-carboxylic acid (150 mg, 0.58 mmol, 97% yield) as a tan glass. MS found: (M+H)+=257.29
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07601844B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-74dde32b171b457f9677f78265380537 |
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| Source note | uspto-grants-2009_10 |
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