HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374261Generated: October 29, 2026
Dimethylformamide → Ethyl 3'-amino-[1,1'-biphenyl]-3-carboxylate
https://huagongshe.com/reaction/1374261
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Ethyl 3-iodobenzoate | HCID 143542 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | Ethyl 3'-amino-[1,1'-biphenyl]-3-carboxylate | HCID 11975548 | 55% |
Reaction Steps
Preparation H3, Step 1: Ethyl 3-iodobenzoate (0.92 g, 3.34 mmol, 1 eq.), phenylboronic acid (0.87 g, 5.02 mmol, 1.5 eq.), palladium(II)acetate (37 mg, 0.167 mmol, 0.05 eq.) and sodium carbonate (706 mg, 6.66 mmol, 2 eq.) were dissolved in DMF (20 mL) at room temperature under nitrogen. The reaction was then heated at 80° C. for 1.5 hours. Worked up by adding ethyl acetate and rinsing 4 times with water. The organic layer was dried over sodium sulfate and stripped to give a dark oil. Purified over silica gel in 9:1 to 1:1 hexanes/ethyl acetate to obtain 3′-Amino-[1,1′-biphenyl]-3-carboxylic acid, ethyl ester (420 mg) as an oil. Yield=55%. LCMS detects (M+H)+=242.41.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07163937B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-7768b81f116745498de24cfadb6f2cc3 |
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| Source note | uspto-grants-2007_01 |
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