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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
ReactantPhenylboronic AcidHCID 66827—
ReactantEthyl 3-iodobenzoateHCID 143542—
Catalystpalladium(II) acetateHCID 167845—
ProductEthyl 3'-amino-[1,1'-biphenyl]-3-carboxylateHCID 1197554855%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163937B2
Source datasetuspto-grants-2007_01
ORD IDord-7768b81f116745498de24cfadb6f2cc3
Source noteuspto-grants-2007_01