HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2410547Generated: November 2, 2026
Cesium fluoride → Methyl 2'-chloro-3'-fluoro-2-(methoxymethyl)biphenyl-4-carboxylate
https://huagongshe.com/reaction/2410547
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Reactant | (2-Chloro-3-fluorophenyl)boronic acid | HCID 22309459 | — |
| Reactant | 3'-Fluoro-2-(methoxymethyl)-2'-methylbiphenyl-4-carboxylic acid | HCID 58066398 | — |
| Reactant | Methyl 4-bromo-3-(methoxymethyl)benzoate | HCID 58554220 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 2'-chloro-3'-fluoro-2-(methoxymethyl)biphenyl-4-carboxylate | HCID 66678433 | — |
Reaction Steps
A mixture of methyl 4-bromo-3-(methoxymethyl)benzoate (Intermediate 1, Step 2, 3.00 g, 11.6 mmol), 2-chloro-3-fluorophenylboronic acid (2.42 g, 13.9 mmol), cesium fluoride (5.27 g, 34.7 mmol), palladium acetate (52 mg, 0.23 mmol) and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (285 mg, 0.69 mmol) was prepared in dioxane (30 mL) and water (15 mL), and then heated at 90° C. for 1 hour. Additional amounts of 2-chloro-3-fluorophenylboronic acid (2.42 g, 13.9 mmol), palladium acetate (52 mg, 0.23 mmol) and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (285 mg, 0.69 mmol) were added, and then the resulting mixture was maintained at 90° C. for 1 additional hour. The reaction mixture was diluted with MTBE (200 mL) and washed with water (2×100 mL) and brine (100 mL). The aqueous layers were extracted with MTBE (100 mL). The organic layers were combined, dried (MgSO4) and treated with activated charcoal. After filtration through a Celite pad, the solution was concentrated under vacuum. After purification by flash chromatography (silica, heptane/EtOAc), the title compound was obtained as a pale yellow oil. HPLC (Method A) Rt 4.9 min (Purity: 99.6%). LC/MS (Method B): 309.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815919B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-bc8a4de914f646e4ba2d4cc81c7cbb91 |
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| Source note | uspto-grants-2014_08 |
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