HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cesium fluoride → Methyl 6-benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | Tolylboronic acid | HCID 79799 | — |
| Reactant | Methyl 4-benzyloxy-3-tert-butyl-5-iodobenzoate | HCID 12084816 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 6-benzyloxy-5-tert-butyl-4'-methyl-3-biphenylcarboxylate | HCID 12084817 | 83% |
Reaction Steps
12 g (28 mmol) of methyl 4-benzyloxy-3-tert-butyl-5-iodobenzoate are dissolved with 5.8 g (42 mmol) of 4-methylbenzeneboronic acid and 12.7 g (84 mmol) of caesium fluoride in 400 mL of dioxane. The reaction medium is degassed with a flow of nitrogen for 15 minutes, and 1.7 g (1.4 mmol) of tetrakis(triphenylphosphine)palladium are then added. The reaction medium is refluxed for 4 hours and then cooled and hydrolysed. After extraction with ethyl acetate, the organic phase is filtered and concentrated. The residue is purified by chromatography (eluent: 98 heptane/2 ethyl acetate): a colorless oil is obtained (m=9 g, yield=83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07468457B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-085ac38486c845cb925cf3f08237060b |
| Source note | uspto-grants-2008_12 |