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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 4-Aminophenylboronic acid | HCID 2734615 | — |
| Reactant | benzyl 2-(5-(4-bromophenyl)tetrahydro-2H-pyran-2-yl)acetate | HCID 89872727 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | benzyl 2-(5-(4'-amino-[1,1'-biphenyl]-4-yl)tetrahydro-2H-pyran-2-yl)acetate | HCID 89872737 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108956B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-6dd5f49507834eb5a1d7cddff8114853 |
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| Source note | uspto-grants-2015_08 |
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