HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1849885Generated: November 2, 2026
Potassium Phosphate, Tribasic → 4-((1-Benzhydrylpiperidin-4-yl)methoxy) 5-cyclopropyl-2-fluorobenzoic acid
https://huagongshe.com/reaction/1849885
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | Tri(cyclohexyl)phosphine tetrafluoroborate | HCID 20066521 | — |
| Reactant | 4-((1-Benzhydrylpiperidin-4-yl)methoxy)-5-chloro-2-fluorobenzoic acid | HCID 86703764 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-((1-Benzhydrylpiperidin-4-yl)methoxy) 5-cyclopropyl-2-fluorobenzoic acid | HCID 86703765 | — |
Reaction Steps
A mixture of 4-((1-benzhydrylpiperidin-4-yl)methoxy)-5-chloro-2-fluorobenzoic acid (480 mg, 0.94 mmol), cyclopropylboronic acid (162 mg, 1.88 mmol), potassium phosphate (797 mg, 3.67 mmol), palladium acetate (21 mg, 0.047 mmol) and tricyclohexylphosphine tetrafluoroborate (36 mg, 0.094 mmol) in toluene (10 mL) and water (0.5 mL) was stirred under a nitrogen atmosphere at 100° C. for 18 h. The reaction mixture was cooled down, quenched with water (50 mL) and extracted with ethyl acetate (20 mL×3). The combined organic layers were washed with brine (20 mL), dried over anhydrous sodium sulfate, filtered and concentrated to afford product (320 mg, 46%, crude) as oil which was used in the next step without further purification. LCMS (ESI) m/z: 458.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08952169B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-7554cdfe36ff4f6ebcab8d8c3332aa14 |
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| Source note | uspto-grants-2015_02 |
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