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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515390Generated: October 31, 2026

Sodium Carbonate → benzyl 2-(5-(4'-amino-[1,1'-biphenyl]-4-yl)tetrahydro-2H-pyran-2-yl)acetate

https://huagongshe.com/reaction/515390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-Aminophenylboronic acidHCID 2734615—
Reactantbenzyl 2-(5-(4-bromophenyl)tetrahydro-2H-pyran-2-yl)acetateHCID 89872727—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
Productbenzyl 2-(5-(4'-amino-[1,1'-biphenyl]-4-yl)tetrahydro-2H-pyran-2-yl)acetateHCID 8987273781%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of benzyl 2-(5-(4-bromophenyl)tetrahydro-2H-pyran-2-yl)acetate (300 mg, 0.771 mmol) in dioxane (6 ml) at room temperature was added 4-aminophenylboronic acid (211 mg, 1.541 mmol), Pd(Ph3P)4 (178 mg, 0.154 mmol) and 2M Na2CO3 (1.541 ml, 3.08 mmol) and the mixture was degassed and heated at 120° C. in microwave for 30 min. The reaction was quenched by sat. aq. NH4Cl and was extracted with EtOAc. The combined organic layer was washed with brine and dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by flash chromatography (10 to 50% EtOAc (2% TEA)/Heptane) to give the title compound 250 mg (yield 81%). MS (ESI) m/z 402.3 (M+1). Retention time 1.48 min (condition A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108956B2
Source datasetuspto-grants-2015_08
ORD IDord-6dd5f49507834eb5a1d7cddff8114853
Source noteuspto-grants-2015_08