HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404335Generated: October 27, 2026
Water → Methyl 2-chloro-2'-(trifluoromethyl)biphenyl-4-carboxylate
https://huagongshe.com/reaction/2404335
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Benzene, 1-bromo-2-(trifluoromethyl)- | HCID 9806 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 2-Chloro-4-(methoxycarbonyl)benzeneboronic acid | HCID 22171291 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 2-chloro-2'-(trifluoromethyl)biphenyl-4-carboxylate | HCID 66718347 | — |
Reaction Steps
A mixture of methyl 4-borono-3-chlorobenzoate (Combi-Blocks BB-3530, 1.5 g, 7.0 mmol), 2-bromobenzotrifluoride (1.9 g, 8.4 mmol), cesium fluoride (3.2 g; 21.0 mmol) and bis(triphenylphosphine)palladium(II) chloride (98 mg, 0.14 mmol) was prepared in dioxane (15 mL) and water (7.5 mL) under nitrogen atmosphere, and then heated at 90° C. for 30 minutes. The reaction mixture was diluted with MTBE (30 mL) and washed with water and brine. The aqueous layers were extracted with MTBE (30 mL). The combined organic layers were dried (MgSO4) and concentrated under vacuum. After two purifications by flash chromatography (silica, heptane/DCM, then heptane/EtOAc), the title compound was obtained as a yellow oil. HPLC (Method A) Rt 5.3 min (Purity: 99.7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802704B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-33f9a1668d9d4ee08d656e807ae48687 |
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| Source note | uspto-grants-2014_08 |
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